GB652830A - Improvements in and relating to insoluble poly-quaternary resins - Google Patents
Improvements in and relating to insoluble poly-quaternary resinsInfo
- Publication number
- GB652830A GB652830A GB2761748A GB2761748A GB652830A GB 652830 A GB652830 A GB 652830A GB 2761748 A GB2761748 A GB 2761748A GB 2761748 A GB2761748 A GB 2761748A GB 652830 A GB652830 A GB 652830A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reacted
- oxygen atom
- dibromide
- hexa
- tetramethyl
- 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
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
- 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
- C08G73/0226—Quaternisation of polyalkylene(poly)amines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
Abstract
Insoluble polyquaternary resins having ion-exchange properties are made by reacting substituted hydrocarbon compounds, the molecules of one containing at least two halide groups with the halogen atoms not closer together than the 1 : 4 position, and those of the other containing at least two tertiary amino groups, there being on the average more than two such functional groups per molecule. The reaction may also be a polymerization of the molecules of a single compound containing both functional groups in the proportions and position specified. The resins are salts which on treatment with an alkali such as caustic soda give the hydroxide which may be used for the absorption or removal of acids or acid vapours. In examples: (1) tri - (dimethylamino -ethyl) - amine is reacted with pentamethylene dibromide; (2) hexa (N-methyl) triethylene tetramine is reacted with tetramethylene dibromide; (3) an aqueous solution of the polyamine of (2) is emulsified with tetramethylene dibromide and heated; (4) the product of (3) is washed with caustic soda; (5) tris-b -bromoethyl-methane is reacted with hexa - (N - methyl) - triethylene tetramine; (6) tetrakis-bromoethyl-ethane is reacted with N,N,N1,N1 - tetramethyl - hexamethylene diamine; (7) para-xylylene dibromide is emulsified with an aqueous solution of hexa - (N-methyl)-triethylene-tetramine and heated; (8) N,N1 - tetramethyl - 4 - hydroxy - 4 - tetrahydropyranyl - heptamethylene - diamine is heated with excess anhydrous HBr to replace the 4-hydroxy group by Br and to displace the oxygen atom from, and break, the pyrane ring and substitute a bromine atom at each of the carbon atoms previously directly bonded to the oxygen atom, the resulting compound being made alkaline, extracted and polymerized by heating.ALSO:In example VIII, a bromine-containing tertiary amine which may be polymerized to give a polyquaternary resin (see Group IV (a)), is made by heating N,N1 - tetramethyl - 4 - hydroxy - 4 - tetrahydropyranyl - heptamethylene-diamine with excess anhydrous HBr to replace the 4-hydroxy group by Br and to displace the oxygen atom from, and break, the pyrane ring and substitute a bromine atom at each of the carbon atoms previously directly bonded to the oxygen atom.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2761748A GB652830A (en) | 1948-10-23 | 1948-10-23 | Improvements in and relating to insoluble poly-quaternary resins |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2761748A GB652830A (en) | 1948-10-23 | 1948-10-23 | Improvements in and relating to insoluble poly-quaternary resins |
Publications (1)
Publication Number | Publication Date |
---|---|
GB652830A true GB652830A (en) | 1951-05-02 |
Family
ID=10262509
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2761748A Expired GB652830A (en) | 1948-10-23 | 1948-10-23 | Improvements in and relating to insoluble poly-quaternary resins |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB652830A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1042236B (en) * | 1954-05-20 | 1958-10-30 | Rohm & Haas | Process for the preparation of bisquaternary polymers of a vinyl aromatic hydrocarbon |
US2898310A (en) * | 1956-08-08 | 1959-08-04 | Pfaudler Permutit Inc | Highly-basic anion exchange resins from epihalohydrins and tertiary - amino containing alkylenepolyamines |
US2912390A (en) * | 1956-05-08 | 1959-11-10 | Pittsburgh Plate Glass Co | Synthetic resin from dihaloalkyl xylene and polyalkylene polyamines |
DE1123468B (en) * | 1955-01-22 | 1962-02-08 | Hermann Leinfelder | Process for the production of water-soluble, poly-N-quaternary substances that increase diffusion in tissues |
DE1207627B (en) * | 1956-01-25 | 1965-12-23 | Onyx Chemical Corp | Process for the production of polycondensates |
US3899534A (en) * | 1971-10-12 | 1975-08-12 | California Inst Of Techn | Cross-linked polyelectrolytes |
US4014955A (en) * | 1973-02-14 | 1977-03-29 | Ciba-Geigy Ag | Process for the manufacture of polyethers containing ionic bonds |
-
1948
- 1948-10-23 GB GB2761748A patent/GB652830A/en not_active Expired
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1042236B (en) * | 1954-05-20 | 1958-10-30 | Rohm & Haas | Process for the preparation of bisquaternary polymers of a vinyl aromatic hydrocarbon |
DE1123468B (en) * | 1955-01-22 | 1962-02-08 | Hermann Leinfelder | Process for the production of water-soluble, poly-N-quaternary substances that increase diffusion in tissues |
DE1207627B (en) * | 1956-01-25 | 1965-12-23 | Onyx Chemical Corp | Process for the production of polycondensates |
US2912390A (en) * | 1956-05-08 | 1959-11-10 | Pittsburgh Plate Glass Co | Synthetic resin from dihaloalkyl xylene and polyalkylene polyamines |
US2898310A (en) * | 1956-08-08 | 1959-08-04 | Pfaudler Permutit Inc | Highly-basic anion exchange resins from epihalohydrins and tertiary - amino containing alkylenepolyamines |
US3899534A (en) * | 1971-10-12 | 1975-08-12 | California Inst Of Techn | Cross-linked polyelectrolytes |
US4014955A (en) * | 1973-02-14 | 1977-03-29 | Ciba-Geigy Ag | Process for the manufacture of polyethers containing ionic bonds |
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