GB835550A - Quaternary ammonium copolymers and methods of producing them - Google Patents
Quaternary ammonium copolymers and methods of producing themInfo
- 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
Links
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
- 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
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/10—Esters
- C08F20/34—Esters containing nitrogen, e.g. N,N-dimethylaminoethyl (meth)acrylate
-
- 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
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/44—Preparation 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.
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)
| 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)
| 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 |
-
1956
- 1956-03-13 GB GB7867/56A patent/GB835550A/en not_active Expired
- 1956-03-20 DE DER18551A patent/DE1118457B/en active Pending
- 1956-03-21 FR FR1148102D patent/FR1148102A/en not_active Expired
Cited By (3)
| 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 |
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