GB1430782A - Process for manufacutring amphoteric ion exchange resins - Google Patents
Process for manufacutring amphoteric ion exchange resinsInfo
- Publication number
- GB1430782A GB1430782A GB2575373A GB2575373A GB1430782A GB 1430782 A GB1430782 A GB 1430782A GB 2575373 A GB2575373 A GB 2575373A GB 2575373 A GB2575373 A GB 2575373A GB 1430782 A GB1430782 A GB 1430782A
- Authority
- GB
- United Kingdom
- Prior art keywords
- monomer
- groups
- derivative
- polymerization
- charged
- 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
- 239000003456 ion exchange resin Substances 0.000 title abstract 3
- 229920003303 ion-exchange polymer Polymers 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 239000000178 monomer Substances 0.000 abstract 9
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 abstract 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- 238000006116 polymerization reaction Methods 0.000 abstract 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 abstract 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 abstract 2
- 230000002378 acidificating effect Effects 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- VPYJNCGUESNPMV-UHFFFAOYSA-N triallylamine Chemical compound C=CCN(CC=C)CC=C VPYJNCGUESNPMV-UHFFFAOYSA-N 0.000 abstract 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 abstract 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 abstract 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 abstract 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003368 amide group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 1
- 125000002843 carboxylic acid group Chemical group 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000004132 cross linking Methods 0.000 abstract 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 abstract 1
- TWRQCVNFACGORI-UHFFFAOYSA-N hexane;dihydrochloride Chemical compound Cl.Cl.CCCCCC TWRQCVNFACGORI-UHFFFAOYSA-N 0.000 abstract 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 abstract 1
- 125000000879 imine group Chemical group 0.000 abstract 1
- 239000003999 initiator Substances 0.000 abstract 1
- 238000005342 ion exchange Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 abstract 1
- WGESLFUSXZBFQF-UHFFFAOYSA-N n-methyl-n-prop-2-enylprop-2-en-1-amine Chemical compound C=CCN(C)CC=C WGESLFUSXZBFQF-UHFFFAOYSA-N 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 230000008520 organization Effects 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000000126 substance Substances 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
- C08F26/00—Homopolymers and 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 single or double bond to nitrogen or by a heterocyclic ring containing nitrogen
- C08F26/02—Homopolymers and 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 single or double bond to nitrogen or by a heterocyclic ring containing nitrogen by a single or double bond to nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J43/00—Amphoteric ion-exchange, i.e. using ion-exchangers having cationic and anionic groups; Use of material as amphoteric ion-exchangers; Treatment of material for improving their amphoteric ion-exchange properties
-
- 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
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/62—Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPA916772 | 1972-05-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1430782A true GB1430782A (en) | 1976-04-07 |
Family
ID=3765089
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2575373A Expired GB1430782A (en) | 1972-05-31 | 1973-05-30 | Process for manufacutring amphoteric ion exchange resins |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3839237A (enExample) |
| JP (1) | JPS5247516B2 (enExample) |
| CA (1) | CA1014694A (enExample) |
| DE (1) | DE2327433A1 (enExample) |
| FR (1) | FR2186497B1 (enExample) |
| GB (1) | GB1430782A (enExample) |
| NL (1) | NL7307444A (enExample) |
| ZA (1) | ZA733409B (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2412092A1 (de) * | 1973-03-13 | 1974-09-26 | Maruzen Oil Co Ltd | Polyionkomplexe, verfahren zu deren herstellung und deren verwendung |
| US3941724A (en) * | 1973-08-09 | 1976-03-02 | Ici Australia Limited | Production of amphoteric resins in a reaction medium comprising formic acid |
| US4087357A (en) * | 1973-12-27 | 1978-05-02 | Rohm And Haas Company | Desalination process using thermally regenerable resins |
| US4121986A (en) * | 1975-05-07 | 1978-10-24 | Ici Australia Limited | Process for the polymerization of polyallylamines in the presence of a mineral acid solution |
| US4134815A (en) * | 1976-05-31 | 1979-01-16 | Ici Australia Limited | Amphoteric composite resins and method of preparing same by polymerization of a two-phase dispersion of monomers |
| US4102876A (en) * | 1977-04-18 | 1978-07-25 | Exxon Research & Engineering Co. | Quaternary phosphonium ionomers |
| JPS53130680A (en) * | 1977-04-20 | 1978-11-14 | Ajinomoto Co Inc | Recovery of nucleotide |
| AU3747378A (en) * | 1977-06-27 | 1980-02-21 | Univ Melbourne | Amphoteric latices |
| US4378439A (en) * | 1978-03-06 | 1983-03-29 | Ici Australia Limited | Purification of saline solutions |
| US4221887A (en) * | 1978-07-17 | 1980-09-09 | Exxon Research & Engineering Co. | Plasticization of quaternary phosphonium ion containing polymers |
| JPS57200366U (enExample) * | 1981-06-18 | 1982-12-20 | ||
| US4706755A (en) * | 1985-05-09 | 1987-11-17 | Ethyl Corporation | Fluid loss control in well cement slurries |
| US4698380A (en) * | 1985-09-23 | 1987-10-06 | Ethyl Corporation | Fluid loss control in well cement slurries |
| US4927896A (en) * | 1986-04-25 | 1990-05-22 | Ethyl Corporation | Process for polymerizing monoallylamine |
| US5053448A (en) * | 1989-07-21 | 1991-10-01 | S. C. Johnson & Son, Inc. | Polymeric thickener and methods of producing the same |
| DE4339635A1 (de) * | 1993-11-26 | 1995-06-22 | Thomas Dipl Chem Schlieper | Verfahren zur Darstellung von Perlpolymeren als Katalysatorträger und deren Dotierung mit Metallverbindungen |
| GB9624130D0 (en) * | 1996-11-20 | 1997-01-08 | Biocompatibles Ltd | Biocompatible compositions |
| US20110198292A1 (en) * | 2010-02-12 | 2011-08-18 | Scarborough Walter W | Desalination of water |
| US10385424B2 (en) * | 2016-01-29 | 2019-08-20 | Deringer-Ney, Inc. | Palladium-based alloys |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2592107A (en) * | 1948-11-19 | 1952-04-08 | Hercules Powder Co Ltd | Synthetic amphoteric polymers containing free amino groups and free acid groups |
| FR1104541A (fr) * | 1954-05-13 | 1955-11-21 | Kodak Pathe | Procédé pour la préparation de hauts polymères, nouveaux produits obtenus et leurs applications |
| US3032539A (en) * | 1956-09-27 | 1962-05-01 | American Cyanamid Co | Copolymers of a bis ethylenically unsaturated amine |
| US3032538A (en) * | 1959-04-28 | 1962-05-01 | Goodrich Co B F | Cross-linked carboxylic polymers |
| US3639208A (en) * | 1968-03-04 | 1972-02-01 | Calgon Corp | Polyamphoteric polymeric retention aids |
-
1973
- 1973-05-21 ZA ZA733409A patent/ZA733409B/xx unknown
- 1973-05-21 US US00362057A patent/US3839237A/en not_active Expired - Lifetime
- 1973-05-29 DE DE2327433A patent/DE2327433A1/de not_active Ceased
- 1973-05-29 NL NL7307444A patent/NL7307444A/xx not_active Application Discontinuation
- 1973-05-30 FR FR7319914A patent/FR2186497B1/fr not_active Expired
- 1973-05-30 GB GB2575373A patent/GB1430782A/en not_active Expired
- 1973-05-31 CA CA172,916A patent/CA1014694A/en not_active Expired
- 1973-05-31 JP JP48061416A patent/JPS5247516B2/ja not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2186497B1 (enExample) | 1977-04-29 |
| JPS5247516B2 (enExample) | 1977-12-02 |
| NL7307444A (enExample) | 1973-12-04 |
| ZA733409B (en) | 1974-05-29 |
| JPS4966795A (enExample) | 1974-06-28 |
| FR2186497A1 (enExample) | 1974-01-11 |
| DE2327433A1 (de) | 1973-12-13 |
| CA1014694A (en) | 1977-07-26 |
| US3839237A (en) | 1974-10-01 |
Similar Documents
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |