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GB652830A - Improvements in and relating to insoluble poly-quaternary resins - Google Patents

Improvements in and relating to insoluble poly-quaternary resins

Info

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
Application number
GB2761748A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to GB2761748A priority Critical patent/GB652830A/en
Publication of GB652830A publication Critical patent/GB652830A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G73/00Macromolecular 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
    • C08G73/02Polyamines
    • C08G73/0206Polyalkylene(poly)amines
    • C08G73/0213Preparatory process
    • C08G73/0226Quaternisation 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.
GB2761748A 1948-10-23 1948-10-23 Improvements in and relating to insoluble poly-quaternary resins Expired GB652830A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (7)

* Cited by examiner, † Cited by third party
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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