GB976570A - Amphoteric ion exchange resins - Google Patents
Amphoteric ion exchange resinsInfo
- Publication number
- GB976570A GB976570A GB3602163A GB3602163A GB976570A GB 976570 A GB976570 A GB 976570A GB 3602163 A GB3602163 A GB 3602163A GB 3602163 A GB3602163 A GB 3602163A GB 976570 A GB976570 A GB 976570A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethylene
- sulphate
- ethylene imine
- imino
- acid
- 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 2
- 229920003303 ion-exchange polymer Polymers 0.000 title abstract 2
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 abstract 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- 239000003054 catalyst Substances 0.000 abstract 3
- DENRZWYUOJLTMF-UHFFFAOYSA-N diethyl sulfate Chemical compound CCOS(=O)(=O)OCC DENRZWYUOJLTMF-UHFFFAOYSA-N 0.000 abstract 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- 239000003995 emulsifying agent Substances 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- -1 sulphonic acid ester Chemical class 0.000 abstract 2
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 abstract 1
- 125000005907 alkyl ester group Chemical group 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 abstract 1
- 229910052788 barium Inorganic materials 0.000 abstract 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000003518 caustics Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 238000007334 copolymerization reaction Methods 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- LMEDOLJKVASKTP-UHFFFAOYSA-N dibutyl sulfate Chemical compound CCCCOS(=O)(=O)OCCCC LMEDOLJKVASKTP-UHFFFAOYSA-N 0.000 abstract 1
- JYCKNDWZDXGNBW-UHFFFAOYSA-N dipropyl sulfate Chemical compound CCCOS(=O)(=O)OCCC JYCKNDWZDXGNBW-UHFFFAOYSA-N 0.000 abstract 1
- 125000004494 ethyl ester group Chemical group 0.000 abstract 1
- 150000002191 fatty alcohols Chemical class 0.000 abstract 1
- 229910052745 lead Inorganic materials 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229910021645 metal ion Inorganic materials 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- IQAVEDGXJROTIJ-UHFFFAOYSA-N methyl 2-iminopropanoate Chemical compound COC(=O)C(C)=N IQAVEDGXJROTIJ-UHFFFAOYSA-N 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
- C07D203/04—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D203/06—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D203/08—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring nitrogen atom
- C07D203/12—Radicals substituted by nitrogen atoms not forming part of a nitro radical
-
- 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
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
-
- 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
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/564—Three-membered rings
-
- 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
- C08G14/00—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00
- C08G14/02—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes
- C08G14/04—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols
- C08G14/06—Condensation polymers of aldehydes or ketones with two or more other monomers covered by at least two of the groups C08G8/00 - C08G12/00 of aldehydes with phenols and monomers containing hydrogen attached to nitrogen
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/0206—Polyalkylene(poly)amines
- C08G73/0213—Preparatory process
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Epoxy Resins (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF30460A DE1160183B (de) | 1960-02-04 | 1960-02-04 | Verfahren zur Herstellung von als amphotere Ionenaustauscher dienenden Copolymerisaten von AEthyleniminverbindungen |
| DEF30457A DE1153022B (de) | 1960-02-04 | 1960-02-04 | Verfahren zur Herstellung von AEthylenimin-N-aethylphosphonsaeure-dialkylestern |
| FR851318A FR1278553A (fr) | 1960-02-04 | 1961-02-01 | Résines amphotères échangeuses d'ions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB976570A true GB976570A (en) | 1964-11-25 |
Family
ID=27210163
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3602163A Expired GB976570A (en) | 1960-02-04 | 1961-02-02 | Amphoteric ion exchange resins |
| GB402261A Expired GB976566A (en) | 1960-02-04 | 1961-02-02 | Amphoteric ion exchange resins |
| GB54363A Expired GB976568A (en) | 1960-02-04 | 1961-02-02 | A process for the production of amphoteric ion exchange resins |
| GB54463A Expired GB976569A (en) | 1960-02-04 | 1961-02-02 | A process for the preparation of diesters of n-dihydroxy-phosphinylethyl ethylene imine |
| GB54263A Expired GB976567A (en) | 1960-02-04 | 1961-02-02 | A process for the production of amphoteric ion exchange resins |
Family Applications After (4)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB402261A Expired GB976566A (en) | 1960-02-04 | 1961-02-02 | Amphoteric ion exchange resins |
| GB54363A Expired GB976568A (en) | 1960-02-04 | 1961-02-02 | A process for the production of amphoteric ion exchange resins |
| GB54463A Expired GB976569A (en) | 1960-02-04 | 1961-02-02 | A process for the preparation of diesters of n-dihydroxy-phosphinylethyl ethylene imine |
| GB54263A Expired GB976567A (en) | 1960-02-04 | 1961-02-02 | A process for the production of amphoteric ion exchange resins |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1160183B (enrdf_load_stackoverflow) |
| FR (1) | FR1278553A (enrdf_load_stackoverflow) |
| GB (5) | GB976570A (enrdf_load_stackoverflow) |
| NL (1) | NL260849A (enrdf_load_stackoverflow) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3459686A (en) * | 1966-06-06 | 1969-08-05 | Dow Chemical Co | Aziridine copolymers |
| US3468818A (en) * | 1966-08-01 | 1969-09-23 | Nalco Chemical Co | Polymers and process of preparation |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1270287B (de) * | 1965-09-27 | 1968-06-12 | Max Planck Gesellschaft | Verfahren zur Herstellung von als amphotere Ionenaustauscher dienenden Copolymerisaten von AEthyleniminverbindungen |
| DE3018862A1 (de) * | 1975-01-27 | 1982-01-21 | A.T. Ramot Plastics Ltd., Tel Aviv | Aromatische araliphatische polymere und copolymere und daraus hergestellte produkte |
| US4020019A (en) | 1975-01-29 | 1977-04-26 | Gianluigi Soldati | Anticaries agents |
| JPS5443292A (en) * | 1977-09-12 | 1979-04-05 | Unitika Ltd | Etherified phenolic chelate resin* its production* and adsorption treatment |
| DE4039920A1 (de) * | 1990-12-14 | 1992-06-17 | Basf Ag | Neue polyethylenimin- und polyvinylamin-derivate, mit diesen derivaten beschichtete traegermaterialien auf der basis von aluminium sowie deren verwendung zur herstellung von offsetdruckplatten |
| CN108479713A (zh) * | 2018-04-10 | 2018-09-04 | 浙江农林大学 | 一种氨基羧酸型水热竹炭合成方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL110743C (enrdf_load_stackoverflow) * | 1954-05-17 | 1900-01-01 | ||
| DE1056825B (de) * | 1956-03-07 | 1959-05-06 | Wolfen Filmfab Veb | Verfahren zur Herstellung von unloeslichen stickstoffhaltigen Kationenaustauscherharzen |
| DE1056371B (de) * | 1956-05-23 | 1959-04-30 | Wolfen Filmfab Veb | Verfahren zur Herstellung von als Anionenaustauscher oder Adsorptionsmittel dienenden Kunstharzen |
-
0
- NL NL260849D patent/NL260849A/xx unknown
-
1960
- 1960-02-04 DE DEF30460A patent/DE1160183B/de active Pending
-
1961
- 1961-02-01 FR FR851318A patent/FR1278553A/fr not_active Expired
- 1961-02-02 GB GB3602163A patent/GB976570A/en not_active Expired
- 1961-02-02 GB GB402261A patent/GB976566A/en not_active Expired
- 1961-02-02 GB GB54363A patent/GB976568A/en not_active Expired
- 1961-02-02 GB GB54463A patent/GB976569A/en not_active Expired
- 1961-02-02 GB GB54263A patent/GB976567A/en not_active Expired
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3459686A (en) * | 1966-06-06 | 1969-08-05 | Dow Chemical Co | Aziridine copolymers |
| US3468818A (en) * | 1966-08-01 | 1969-09-23 | Nalco Chemical Co | Polymers and process of preparation |
Also Published As
| Publication number | Publication date |
|---|---|
| GB976568A (en) | 1964-11-25 |
| GB976569A (en) | 1964-11-25 |
| DE1160183B (de) | 1963-12-27 |
| GB976567A (en) | 1964-11-25 |
| FR1278553A (fr) | 1961-12-08 |
| GB976566A (en) | 1964-11-25 |
| NL260849A (enrdf_load_stackoverflow) |
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