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 useInfo
- 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
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 15
- 239000006185 dispersion Substances 0.000 title abstract 13
- 239000000839 emulsion Substances 0.000 title abstract 13
- 229920005989 resin Polymers 0.000 title abstract 3
- 239000011347 resin Substances 0.000 title abstract 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 title abstract 3
- 229920002554 vinyl polymer Polymers 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 16
- 238000000576 coating method Methods 0.000 abstract 12
- 229920000642 polymer Polymers 0.000 abstract 10
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical group N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 8
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 8
- 238000006116 polymerization reaction Methods 0.000 abstract 8
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical group COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 6
- 239000003795 chemical substances by application Substances 0.000 abstract 6
- 238000001704 evaporation Methods 0.000 abstract 6
- 230000008020 evaporation Effects 0.000 abstract 6
- 239000003921 oil Substances 0.000 abstract 6
- 150000003839 salts Chemical class 0.000 abstract 6
- 239000002023 wood Substances 0.000 abstract 6
- PQUXFUBNSYCQAL-UHFFFAOYSA-N 1-(2,3-difluorophenyl)ethanone Chemical compound CC(=O)C1=CC=CC(F)=C1F PQUXFUBNSYCQAL-UHFFFAOYSA-N 0.000 abstract 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 abstract 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract 4
- 239000004902 Softening Agent Substances 0.000 abstract 4
- 229920002125 Sokalan® Polymers 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 4
- 150000007513 acids Chemical class 0.000 abstract 4
- RGCKGOZRHPZPFP-UHFFFAOYSA-N alizarin Chemical compound C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 abstract 4
- 229910021529 ammonia Inorganic materials 0.000 abstract 4
- 239000002184 metal Substances 0.000 abstract 4
- 229910052751 metal Inorganic materials 0.000 abstract 4
- 150000004702 methyl esters Chemical class 0.000 abstract 4
- 239000004584 polyacrylic acid Substances 0.000 abstract 4
- 239000005336 safety glass Substances 0.000 abstract 4
- 229940047670 sodium acrylate Drugs 0.000 abstract 4
- 239000000243 solution Substances 0.000 abstract 4
- 239000002904 solvent Substances 0.000 abstract 4
- 239000000126 substance Substances 0.000 abstract 4
- 241000854350 Enicospilus group Species 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- 229940037003 alum Drugs 0.000 abstract 2
- 239000003153 chemical reaction reagent Substances 0.000 abstract 2
- 238000004040 coloring Methods 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 238000010790 dilution Methods 0.000 abstract 2
- 239000012895 dilution Substances 0.000 abstract 2
- 238000007598 dipping method Methods 0.000 abstract 2
- 238000004945 emulsification Methods 0.000 abstract 2
- 150000002170 ethers Chemical class 0.000 abstract 2
- 125000004494 ethyl ester group Chemical group 0.000 abstract 2
- 239000011521 glass Substances 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- 238000010438 heat treatment Methods 0.000 abstract 2
- 239000011810 insulating material Substances 0.000 abstract 2
- 239000004922 lacquer Substances 0.000 abstract 2
- 239000010985 leather Substances 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 150000002894 organic compounds Chemical class 0.000 abstract 2
- 238000010422 painting Methods 0.000 abstract 2
- 239000000123 paper Substances 0.000 abstract 2
- 150000003021 phthalic acid derivatives Chemical class 0.000 abstract 2
- 239000011148 porous material Substances 0.000 abstract 2
- 239000000344 soap Substances 0.000 abstract 2
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 2
- 230000008961 swelling Effects 0.000 abstract 2
- 239000004753 textile Substances 0.000 abstract 2
- 229920001567 vinyl ester resin Polymers 0.000 abstract 2
- 229920003176 water-insoluble polymer Polymers 0.000 abstract 2
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
- C08F20/62—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
- C08F6/00—Post-polymerisation treatments
- C08F6/14—Treatment of polymer emulsions
- C08F6/20—Concentration
-
- 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
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)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
- Compositions Of Macromolecular Compounds (AREA)
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.
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)
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)
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 |
-
1934
- 1934-04-26 GB GB1266434A patent/GB437446A/en not_active Expired
-
1935
- 1935-04-03 DE DER93018D patent/DE733995C/en not_active Expired
- 1935-04-20 FR FR789166D patent/FR789166A/en not_active Expired
Cited By (9)
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 |
---|---|
FR789166A (en) | 1935-10-24 |
DE733995C (en) | 1943-04-06 |
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