GB437446A - Improvements in or relating to aqueous vinyl resin dispersions or emulsions and to their manufacture and use - Google Patents

Improvements in or relating to aqueous vinyl resin dispersions or emulsions and to their manufacture and use

Info

Publication number
GB437446A
GB437446A GB1266434A GB1266434A GB437446A GB 437446 A GB437446 A GB 437446A GB 1266434 A GB1266434 A GB 1266434A GB 1266434 A GB1266434 A GB 1266434A GB 437446 A GB437446 A GB 437446A
Authority
GB
United Kingdom
Prior art keywords
water
production
groups
coatings
concentration
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
GB1266434A
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.)
Roehm and Haas GmbH
Original Assignee
Roehm and Haas GmbH
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 Roehm and Haas GmbH filed Critical Roehm and Haas GmbH
Priority to GB1266434A priority Critical patent/GB437446A/en
Priority to DER93018D priority patent/DE733995C/en
Priority to FR789166D priority patent/FR789166A/en
Publication of GB437446A publication Critical patent/GB437446A/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
    • C08F20/62Monocarboxylic 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
    • C08F6/00Post-polymerisation treatments
    • C08F6/14Treatment of polymer emulsions
    • C08F6/20Concentration
    • 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

Abstract

Stable, highly concentrated (i.e. over 30 per cent, e.g. 50--65 per cent) aqueous dispersions or emulsions of water-insoluble polymers or mixed polymers of unsaturated organic compounds containing one olefinic double linkage, e.g. acrylic acid and its homologues and derivatives thereof, vinyl esters, ethers and halides and styrols, are manufactured by concentrating an aqueous dispersion or emulsion of one or more of the said polymers containing one or more hydrophile groups (i.e. groups which give rise to water solubility in soaps, e.g. the groups COO Na, COOK and COONH4) in the substances constituting the disperse phase. The hydrophile group or groups may be introduced into the molecule of the polymer or polymers before, during or after polymerization. Thus the polymerization of emulsions of monomeric bodies may be carried out in the presence of small quantities of unsaturated substances containing hydrophile groups, such as water soluble monomeric salts of polymerizable acids, e.g. sodium acrylate. Alternatively compounds containing saponifiable groups may be partially saponified by the action of relatively small quantities of alkali before, during or after polymerization or emulsification. The concentration may be effected by centrifuging or by evaporation or both, if desired with the assistance of further chemical reagents. Specifically heavy solvents or swelling agents for the polymers may be added before concentration, whilst softening agents, e.g. phthalic acid esters, natural and artificial resins, oils, dyestuffs or other colouring matters and solvents may be added before, during or after polymerization and/or concentration. The products, if necessary after dilution with water to the desired viscosity may be employed for the production of coatings or layers on suitable surfaces, e.g. wood, metal, glass, leather or paper, for the production of films, e.g. for safety glass, for the production of intermediate layers of all kinds, as lacquers, impregnating agents for textiles and other porous material and for the production of electrical insulating materials. The films and coatings may be rendered resistant to water by treatment with acids or solution of salts which form water-insoluble salts with the hydrophile groups. In examples: (1) acrylic acid methyl and ethyl esters are polymerized in emulsion in water containing Turkey red oil, hydrogen peroxide and sodium acrylate, and the resulting dispersion is centrifuged; (2) a 25 per cent dispersion of polyacrylic acid methyl ester is warmed with a small amount of caustic soda and then centrifuged; the product, diluted to 50 per cent concentration, is suitable for the production of coatings on wood or other surfaces by painting or dipping; (3) as in (2) except that the concentration is effected by evaporation in vacuo; the product may be employed for the production of coatings on wood, metal and other materials which coatings may be rendered less sensitive to water by treatment with alum solution or dilute hydrochloric acid; (4) as in (3) except that the saponifying agent is ammonia; films and coatings from the product may be made resistant to water by heating; (5) acrylic acid methyl ester is polymerized in emulsion in water containing Turkey red oil, hydrogen peroxide and acrylic acid and the product is neutralized with ammonia and concentrated by evaporation in vacuo. The Provisional Specification comprises also the concentration of the emulsions or dispersions by mechanical means alone. In an additional example, a 25 per cent dispersion of polyacrylic acid methyl ester is shaken up with a softening agent and then centrifuged. The product is suitable for the production of films, especially for safety glass.ALSO:Stable, highly concentrated (i.e. over 30 per cent. e.g. 50--65 per cent) aqueous dispersions or emulsions of water-insoluble polymers or mixed polymers of unsaturated organic compounds containing one olefinic double linkage, e.g. acrylic acid and its homologues and derivatives thereof, vinyl esters, ethers and halides and styrols, are manufactured by concentrating an aqueous dispersion or emulsion of one or more of the said polymers containing one or more hydrophile groups (i.e. groups which give rise to water solubility in soaps, e.g. the groups COONa, COOK and COONH4) in the substances constituting the disperse phase. The hydrophile group or groups may be introduced into the molecule of the polymer or polymers before, during or after polymerization. Thus the polymerization of emulsions of monomeric bodies may be carried out in the presence of small quantities of unsaturated substances containing hydrophile groups, such as water soluble monomeric salts of polymerizable acids, e.g. sodium acrylate. Alternatively compounds containing saponifiable groups may be partially saponified by the action of relatively small quantities of alkali before, during or after polymerization or emulsification. The concentration may be effected by centrifuging or by evaporation or both, if desired with the assistance of further chemical reagents. Specifically heavy solvents or swelling agents for the polymers may be added before concentration, whilst softening agents, e.g. phthalic acid esters, natural and artificial resins, oils, dyestuffs or other colouring matters and solvents may be added before, during or after polymerization and/or concentration. The products, if necessary after dilution with water to the desired biscosity, may be employed for the production of coatings or layers on suitable surfaces, e.g. wood, metal, glass, leather or paper, for the production of films, e.g. for safety glass, for the production of intermediate layers of all kinds, as lacquers, impregnating agents for textiles and other porous material and for the production of electrical insulating materials. The films and coatings may be rendered resistant to water by treatment with acids or solutions of salts which form water-insoluble salts with the hydrophile groups. In example: (1) acrylic acid methyl and ethyl esters are polymerized in emulsion in water containing turkey red oil, hydrogen peroxide and sodium acrylate, and the resulting dispersion is centrifuged; (2) a 25 per cent dispersion of polyacrylic acid methyl ester is warmed with a small amount of caustic soda and then centrifuged; the product, diluted to 50 per cent concentration, is suitable for the production of coatings on wood or other surfaces by painting or dipping; (3) as in (2) except that the concentration is effected by evaporation in vacuo; the product may be employed for the production of coatings on wood, metal and other materials, which coatings may be rendered less sensitive to water by treatment with alum solution or dilute hydrochloric acid; (4) as in (3) except that the saponifying agent is ammonia; films and coatings from the product may be made resistant to water by heating; (5) acrylic acid methyl ester is polymerized in emulsion in water containing turkey red oil, hydrogen peroxide and acrylic acid and the product is neutralized with ammonia and concentrated by evaporation in vacuo. The Provisional Specification comprises also the concentration of the emulsions or dispersions by mechanical means alone. In an additional example, a 25 per cent dispersion of polyacrylic acid methyl ester is shaken up with a softening agent and then centrifuged. The product is suitable for the production of films, especially for safety glass.
GB1266434A 1934-04-26 1934-04-26 Improvements in or relating to aqueous vinyl resin dispersions or emulsions and to their manufacture and use Expired GB437446A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB1266434A GB437446A (en) 1934-04-26 1934-04-26 Improvements in or relating to aqueous vinyl resin dispersions or emulsions and to their manufacture and use
DER93018D DE733995C (en) 1934-04-26 1935-04-03 Process for the production of stable, highly concentratable aqueous dispersions from water-insoluble emulsion polymers of acrylic or vinyl resins
FR789166D FR789166A (en) 1934-04-26 1935-04-20 Vinyl resin dispersions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1266434A GB437446A (en) 1934-04-26 1934-04-26 Improvements in or relating to aqueous vinyl resin dispersions or emulsions and to their manufacture and use

Publications (1)

Publication Number Publication Date
GB437446A true GB437446A (en) 1935-10-28

Family

ID=10008857

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1266434A Expired GB437446A (en) 1934-04-26 1934-04-26 Improvements in or relating to aqueous vinyl resin dispersions or emulsions and to their manufacture and use

Country Status (3)

Country Link
DE (1) DE733995C (en)
FR (1) FR789166A (en)
GB (1) GB437446A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE743945C (en) * 1940-06-12 1944-01-06 Ig Farbenindustrie Ag Process for the production of films, coatings, impregnations and the like like
DE744318C (en) * 1940-07-26 1944-06-17 Ig Farbenindustrie Ag Process for the production of high percentage stable emulsions
US2528469A (en) * 1948-02-24 1950-10-31 Shell Dev Granular polymerization of vinyl chloride
DE751576C (en) * 1936-08-29 1953-02-23 Aeg Electrical conductor with an insulating coating produced by applying an insulating varnish
US2671065A (en) * 1950-03-30 1954-03-02 Minnesota Mining & Mfg Polyvinyl acetate dispersion and method of making utilizing polyacrylic acid and monomer soluble and monomer insoluble catalyst
US2727835A (en) * 1952-07-31 1955-12-20 Monsanto Chemicals Process of sizing synthetic yarn with hydrolyzed polyalkyl acrylates
US2827385A (en) * 1954-10-25 1958-03-18 Bruce E L Co Quick seiting cement
US4030970A (en) * 1973-05-31 1977-06-21 Sanyo Chemical Industries, Ltd. Surface sizing of paper with an acrylic copolymer where scum formation is minimized
US4115331A (en) * 1973-05-31 1978-09-19 Sanyo Chemical Industries, Ltd. Surface sizing compositions for paper

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE980059C (en) * 1951-04-09 1970-09-10 Ciba Geigy Process for the production of acidic, stable, aqueous dispersions of at least internal copolymers
DE1009809B (en) * 1954-11-10 1957-06-06 Basf Ag Process for the production of polyvinyl betaines
US3029225A (en) * 1956-02-20 1962-04-10 Bjorksten Res Lab Inc Temperature and solvent resistance of elastomers

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE751576C (en) * 1936-08-29 1953-02-23 Aeg Electrical conductor with an insulating coating produced by applying an insulating varnish
DE743945C (en) * 1940-06-12 1944-01-06 Ig Farbenindustrie Ag Process for the production of films, coatings, impregnations and the like like
DE744318C (en) * 1940-07-26 1944-06-17 Ig Farbenindustrie Ag Process for the production of high percentage stable emulsions
US2528469A (en) * 1948-02-24 1950-10-31 Shell Dev Granular polymerization of vinyl chloride
US2671065A (en) * 1950-03-30 1954-03-02 Minnesota Mining & Mfg Polyvinyl acetate dispersion and method of making utilizing polyacrylic acid and monomer soluble and monomer insoluble catalyst
US2727835A (en) * 1952-07-31 1955-12-20 Monsanto Chemicals Process of sizing synthetic yarn with hydrolyzed polyalkyl acrylates
US2827385A (en) * 1954-10-25 1958-03-18 Bruce E L Co Quick seiting cement
US4030970A (en) * 1973-05-31 1977-06-21 Sanyo Chemical Industries, Ltd. Surface sizing of paper with an acrylic copolymer where scum formation is minimized
US4115331A (en) * 1973-05-31 1978-09-19 Sanyo Chemical Industries, Ltd. Surface sizing compositions for paper

Also Published As

Publication number Publication date
DE733995C (en) 1943-04-06
FR789166A (en) 1935-10-24

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