[go: up one dir, main page]

GB835550A - Quaternary ammonium copolymers and methods of producing them - Google Patents

Quaternary ammonium copolymers and methods of producing them

Info

Publication number
GB835550A
GB835550A GB7867/56A GB786756A GB835550A GB 835550 A GB835550 A GB 835550A GB 7867/56 A GB7867/56 A GB 7867/56A GB 786756 A GB786756 A GB 786756A GB 835550 A GB835550 A GB 835550A
Authority
GB
United Kingdom
Prior art keywords
group
acrylic
copolymers
methacrylic acid
formula
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
GB7867/56A
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.)
Rohm and Haas Co
Original Assignee
Rohm and Haas Co
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 Rohm and Haas Co filed Critical Rohm and Haas Co
Publication of GB835550A publication Critical patent/GB835550A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers 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
    • C08F20/02Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/10Esters
    • C08F20/34Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00Homopolymers 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
    • C08F20/62Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F8/00Chemical modification by after-treatment
    • C08F8/44Preparation of metal salts or ammonium salts

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Flocculating and aggregating agents comprise copolymers of a quaternary ammonium ester or amide of acrylic or methacrylic acid, one or more derivatives of acrylic or methacrylic acid containing a carbonamido group N-substituted by a methylol or alkoxymethyl group and, optionally, another copolymerizable monomer (see Group IV (a)). Specifications 747,184 and 764,147 are referred to.ALSO:Textile materials, e.g. those made from cotton, cellulose acetate, cellulose acetobutyrate, polyamides, polyethylene terephthalate, acrylonitrile polymers and other vinyl polymers (listed) have applied thereto, in the form of a solution in a liquid vehicle, a copolymer of a quaternary ammonium ester or amide of acrylic or methacrylic acid, one or more derivatives of acrylic or methacrylic acid containing a carbonamido group N-substituted by a methylol or alkoxymethyl group and, optionally, another copolymerizable monomer (see Group IV (a)). Also present may be starches, glue and casein. The copolymer may function as an anti-static agent when applied to textile materials of hydrophobic types or as a softening agent when applied to textile materials of cellulosic types. After application the substrate is usually heated to a temperature of from 212 DEG to 300 DEG F. to dry the applied composition and insolubilize the copolymer. In Examples (6), (7) and (8), processes are described in which the tendency of textile materials made from nylon, polyethylene terephthalate and an acrylonitrile copolymer to develop static charges is reduced by the application thereto of aqueaus solutions of specified copolymers, followed by heating to 300 DEG F. Specifications 747,184 and 764,417 are referred to.ALSO:Copolymers are made containing at least 30 mol. per cent of units represented by formula I below and at least 5 mol. per cent of units represented by the formulae II and/or III below <FORM:0835550/IV (a)/1> wherein R is hydrogen or methyl; Y is a -CONR- or -COO- group; A is a straight-chain or branched-chain alkylene group having 2 to 10 carbon atoms which may be substituted by one or more hydroxyl groups, at least two of the carbon atoms thereof being connected in a chain between the N atom and the Y group of the formula; R1 and R2, when not connected together, each represent a saturated or ethylenically unsaturated hydrocarbon group having 1 to 4 carbon atoms; R1 and R2, when connected together, collectively represent the morpholino residue: (C2H4)2O, the pyrrolidino residue -C4H8-, the piperidino residue -C5H10-, or an N-alkyl piperazino residue: (C2H4)2: NR0, where R0 is a C1-C18 alkyl group; R3 is benzyl or a saturated or ethylenically unsaturated hydrocarbon group of 1 to 4 carbon atoms; and X is a negative, salt-forming atom or radical; <FORM:0835550/IV (a)/2> wherein R is hydrogen or methyl, and R4 is a methylol or alkoxymethyl group. <FORM:0835550/IV (a)/3> wherein R, Y and A are as defined above, and R5 is a -NHCONHR4 group or a group <FORM:0835550/IV (a)/4> in which the radical R4 is as defined above. Also present in the copolymers may be up to 65 mol. per cent of one or more comonomers such as acrylonitrile and its methyl, ethyl and phenyl derivatives, styrene, isopropenyl toluene, dialkyl styrenes, the N-mono- and N-dimethyl, -ethyl, -propyl, -butyl and -phenyl acrylamides and methacrylamides, vinyl acetate, propionate, butyrate, isobutyrate and valerate, the methyl, ethyl, propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, amyl, hexyl, heptyl, octyl, decyl and dodecyl esters of acrylic, methacrylic, ethacrylic and phenylacrylic acids, N-vinyl pyrrolidone, ethylene, vinylidene fluoride and vinyl ethers, e.g. methyl, butyl, aminoisobutyl, formamidoethyl, N-methyl or N-dimethyl amidoethyl and ureidoethyl vinyl ethers and other ureidoalkyl ethers mentioned in Specification 747,184. The copolymers may be prepared by the following methods: (a) by copolymerizing a quaternary ammonium monomer corresponding to formula I with at least one monomer corresponding to formula II and/or III with the aid of initiators such as hydrogen peroxide or a mixture of a persulphate and a hydrosulphite; (b) by copolymerizing a tertiary amino monomer with at least one monomer corresponding to formula II and/or III and quaternizing the resulting copolymer to provide units of formula I; (c) a modification of processes (a) and (b) wherein, instead of monomers corresponding to formula II and/or III, there are used monomers free from methylol or alkoxymethyl groups, which groups are introduced after formation of the copolymer by reaction with formaldehyde followed, optionally, by reaction with an alkanol to provide units of formula II and/or III; and (d) in the case of copolymers containing units of formulae I and III, by aminolysing a polymer of an ester of acrylic or methacrylic ester with a mixture of amines of the formulae <FORM:0835550/IV (a)/5> in which the symbols are as defined above, and quaternizing the resulting product, or alternatively by employing amines free from methylol or alkoxymethyl groups, which groups are introduced subsequently. The copolymers, which are heat-curable, may be used as insecticides, bactericides and fungicides, as antistatic agents for the treatment of hydrophobic plastic materials, as sizes for textile materials, as additives to spinning solutions of cellulose acetate and polyacrylonitrile to improve the dyeing of products formed from such materials, as additives to paper pulp and as flocculating and aggregating agents. Specification 764,147 also is referred to.ALSO:Agents in the purification of water comprise copolymers of a quaternary ammonium ester or amide of acrylic or methacrylic acid, one or more derivatives of acrylic or methacrylic acid containing a carbonamido group N-substituted by a methylol or alkoxymethyl group and, optionally, another copolymerisable monomer (see Group IV(a)). Specifications 747,184 and 764,147 are referred to.ALSO:As flocculating and aggregating agents in the concentration of ores there are used copolymers of a quaternary ammonium ester or amide of acrylic or methacrylic acid, one or more derivatives of acrylic or methacrylic acid containing a carbonamide group N-substituted by a methylol or alkoxymethyl group and, optionally, another copolymerizable monomer (see Group IV(a)). Specifications 747,184 and 764,147 are referred to.
GB7867/56A 1955-03-21 1956-03-13 Quaternary ammonium copolymers and methods of producing them Expired GB835550A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US835550XA 1955-03-21 1955-03-21

Publications (1)

Publication Number Publication Date
GB835550A true GB835550A (en) 1960-05-25

Family

ID=22179086

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7867/56A Expired GB835550A (en) 1955-03-21 1956-03-13 Quaternary ammonium copolymers and methods of producing them

Country Status (3)

Country Link
DE (1) DE1118457B (en)
FR (1) FR1148102A (en)
GB (1) GB835550A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2254021A (en) * 1991-03-28 1992-09-30 Fospur Ltd Froth flotation
EP0964878A4 (en) * 1997-03-03 2004-12-22 Dionex Corp Hydrolytically stable resins for use in anion-exchange chromatography

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SE375780B (en) * 1970-01-30 1975-04-28 Gaf Corp
US3928269A (en) * 1974-09-09 1975-12-23 Phillips Petroleum Co Acid dyeable olefin polymer containing quaternized amine groups
US4014645A (en) * 1975-10-08 1977-03-29 Rohm And Haas Company Dyeable polyolefin backing for tufted surface coverings

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2254021A (en) * 1991-03-28 1992-09-30 Fospur Ltd Froth flotation
GB2254021B (en) * 1991-03-28 1994-07-13 Fospur Ltd Froth flotation of fine coal or mineral particles
EP0964878A4 (en) * 1997-03-03 2004-12-22 Dionex Corp Hydrolytically stable resins for use in anion-exchange chromatography

Also Published As

Publication number Publication date
DE1118457B (en) 1961-11-30
FR1148102A (en) 1957-12-04

Similar Documents

Publication Publication Date Title
US2843573A (en) New quaternary ammonium compounds in which the nitrogen atom carries an alkoxymethyl group
US2980657A (en) Quaternary ammonium compounds of polymers of acrylamido type and methods for making them
US2718515A (en) Copolymers of n-substituted acrylamides
US2891025A (en) Copolymer of acrylonitrile and a quaternary imidazolium compound, method of making same, and a spinning solution thereof
GB839856A (en) Unsaturated thioureido ethers, polymers thereof and process of making them
US2677679A (en) Quaternary ammonium polymers of the acrylic type
US2881155A (en) Polymers of substituted heterocyclic urea compounds
GB835550A (en) Quaternary ammonium copolymers and methods of producing them
GB786960A (en) Polymeric amidoximes
ATE87634T1 (en) WATER-SOLUBLE OR WATER-DISPERSABLE GROSS POLYMERS, THEIR PRODUCTION AND USE.
GB831049A (en) Improvements in and relating to polyacrylonitrile solutions
US3575903A (en) Antistatic compositions of polystyrenes and n-oxyethylated alkylamines
US2490756A (en) N-alkenyl lactamides
GB919317A (en) Sizing solution for glass fibers
GB812140A (en) Improvements in linear copolymers
GB838817A (en) New vinyl heterocyclic nitrogen compounds and polymers thereof
US3035031A (en) Acrylonitrile copolymers
GB902628A (en) Process for the polymerisation of basic compounds
US2850487A (en) Copolymers of acrylonitrile and the mono-amide of guanazole and betacyano-acrylic acid
US2626946A (en) Polymerizable and polymerized acrylonitrile compositions
US2977341A (en) Polymers of vinyl pyridinium betaines
US3179638A (en) Copolymers prepared from vinyl isothiouronium salts and copolymerizable monoethylenically unsaturated monomers
GB785386A (en) Guanamines
US2728739A (en) Polymers of n-acrylylpyrrolidine
US2942021A (en) Tri-nu-propanolamine borate