CH402410A - Verfahren zur Herstellung einer Polymer-Dispersion - Google Patents
Verfahren zur Herstellung einer Polymer-DispersionInfo
- Publication number
- CH402410A CH402410A CH525661A CH525661A CH402410A CH 402410 A CH402410 A CH 402410A CH 525661 A CH525661 A CH 525661A CH 525661 A CH525661 A CH 525661A CH 402410 A CH402410 A CH 402410A
- Authority
- CH
- Switzerland
- Prior art keywords
- dispersion
- polymer
- chain terminator
- added
- sep
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 28
- 238000002360 preparation method Methods 0.000 title claims description 3
- 239000004815 dispersion polymer Substances 0.000 title description 3
- 229920000642 polymer Polymers 0.000 claims description 43
- 239000006185 dispersion Substances 0.000 claims description 35
- 239000007788 liquid Substances 0.000 claims description 29
- 239000000178 monomer Substances 0.000 claims description 20
- 229920001400 block copolymer Polymers 0.000 claims description 19
- 229920000578 graft copolymer Polymers 0.000 claims description 19
- 238000006116 polymerization reaction Methods 0.000 claims description 18
- 230000015572 biosynthetic process Effects 0.000 claims description 13
- -1 alkyl mercaptan Chemical compound 0.000 claims description 12
- 229920001059 synthetic polymer Polymers 0.000 claims description 5
- 239000003381 stabilizer Substances 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 230000000379 polymerizing effect Effects 0.000 claims description 3
- 150000003505 terpenes Chemical class 0.000 claims description 3
- 235000007586 terpenes Nutrition 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 230000003111 delayed effect Effects 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 238000000576 coating method Methods 0.000 claims 1
- 230000001419 dependent effect Effects 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 21
- 239000002245 particle Substances 0.000 description 20
- 239000000203 mixture Substances 0.000 description 12
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 10
- 239000008199 coating composition Substances 0.000 description 9
- 238000010992 reflux Methods 0.000 description 9
- 238000009826 distribution Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- 239000007787 solid Substances 0.000 description 7
- 239000004342 Benzoyl peroxide Substances 0.000 description 6
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 6
- 235000019400 benzoyl peroxide Nutrition 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 230000008719 thickening Effects 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 4
- 239000011362 coarse particle Substances 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- KJRCEJOSASVSRA-UHFFFAOYSA-N propane-2-thiol Chemical compound CC(C)S KJRCEJOSASVSRA-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920002857 polybutadiene Polymers 0.000 description 2
- 230000003678 scratch resistant effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- SFPNZPQIIAJXGL-UHFFFAOYSA-N 2-ethoxyethyl 2-methylprop-2-enoate Chemical compound CCOCCOC(=O)C(C)=C SFPNZPQIIAJXGL-UHFFFAOYSA-N 0.000 description 1
- FRQQKWGDKVGLFI-UHFFFAOYSA-N 2-methylundecane-2-thiol Chemical compound CCCCCCCCCC(C)(C)S FRQQKWGDKVGLFI-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical class [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- IEPRKVQEAMIZSS-UHFFFAOYSA-N Di-Et ester-Fumaric acid Natural products CCOC(=O)C=CC(=O)OCC IEPRKVQEAMIZSS-UHFFFAOYSA-N 0.000 description 1
- IEPRKVQEAMIZSS-WAYWQWQTSA-N Diethyl maleate Chemical compound CCOC(=O)\C=C/C(=O)OCC IEPRKVQEAMIZSS-WAYWQWQTSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZWWQRMFIZFPUAA-UHFFFAOYSA-N dimethyl 2-methylidenebutanedioate Chemical compound COC(=O)CC(=C)C(=O)OC ZWWQRMFIZFPUAA-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000012263 liquid product Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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
- C08F2/00—Processes of polymerisation
- C08F2/04—Polymerisation in solution
- C08F2/06—Organic solvent
- C08F2/08—Organic solvent with the aid of dispersing agents for the polymer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B02—CRUSHING, PULVERISING, OR DISINTEGRATING; PREPARATORY TREATMENT OF GRAIN FOR MILLING
- B02C—CRUSHING, PULVERISING, OR DISINTEGRATING IN GENERAL; MILLING GRAIN
- B02C13/00—Disintegrating by mills having rotary beater elements ; Hammer mills
- B02C13/02—Disintegrating by mills having rotary beater elements ; Hammer mills with horizontal rotor shaft
- B02C13/04—Disintegrating by mills having rotary beater elements ; Hammer mills with horizontal rotor shaft with beaters hinged to the rotor; Hammer mills
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/924—Treating or preparing a nonaqueous solution of a solid polymer or specified intermediate condensation product
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31641—Next to natural rubber, gum, oil, rosin, wax, bituminous or tarry residue
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31645—Next to addition polymer from unsaturated monomers
- Y10T428/31649—Ester, halide or nitrile of addition polymer
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1583260A GB994867A (en) | 1960-05-04 | 1960-05-04 | Dispersion polymerisation |
GB1583060A GB990154A (en) | 1960-05-04 | 1960-05-04 | Dispersion polymerisation |
Publications (1)
Publication Number | Publication Date |
---|---|
CH402410A true CH402410A (de) | 1965-11-15 |
Family
ID=26251572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH525661A CH402410A (de) | 1960-05-04 | 1961-05-04 | Verfahren zur Herstellung einer Polymer-Dispersion |
Country Status (6)
Country | Link |
---|---|
US (2) | US3257340A (en, 2012) |
BE (1) | BE603339A (en, 2012) |
CH (1) | CH402410A (en, 2012) |
LU (2) | LU40084A1 (en, 2012) |
MY (2) | MY6500171A (en, 2012) |
NL (2) | NL264411A (en, 2012) |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
USRE29118E (en) * | 1963-02-06 | 1977-01-18 | Method of preparing polyurethanes from liquid, stable, reactive, film-forming polymer/polyol mixtures formed by polymerizing an ethylenically unsaturated monomer in a polyol | |
DE1495774C3 (de) * | 1964-02-08 | 1974-03-07 | Farbwerke Hoechst Ag, Vormals Meister Lucius & Bruening, 6000 Frankfurt | Verfahren zur Herstellung von Pfropfmischpolymerisaten |
USRE28715E (en) * | 1964-08-12 | 1976-02-17 | Polyurethanes, reactive solutions and methods and their production | |
US3875091A (en) * | 1971-06-25 | 1975-04-01 | Dainippon Toryo Kk | Synthetic polymer dispersions and process for preparation thereof |
US3953393A (en) * | 1974-01-07 | 1976-04-27 | Basf Wyandotte Corporation | Low temperature process for the preparation of graft copolymer dispersions |
JPS557855A (en) * | 1978-07-04 | 1980-01-21 | Nippon Oil & Fats Co Ltd | Preparation of non-aqueous polymer dispersion |
DE3333861A1 (de) * | 1983-09-20 | 1985-04-04 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V., 3400 Göttingen | Strahlungsempfindliches polymermaterial |
US6051633A (en) * | 1991-01-07 | 2000-04-18 | The Sherwin-Williams Company | Non-aqueous dispersions |
US6495618B1 (en) | 1999-12-17 | 2002-12-17 | E. I. Du Pont De Nemours And Company | Graft copolymer with an amide functional group as a pigment dispersant |
US6472463B1 (en) | 1999-12-17 | 2002-10-29 | E. I. Du Pont De Nemours And Company | Graft copolymer pigment dispersant |
US7396879B2 (en) * | 2005-02-22 | 2008-07-08 | Fina Technology, Inc. | Method for reducing residual monomer in a polymer matrix |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA554596A (en) * | 1958-03-18 | A. Hayes Robert | Ternary blend of styrene and butadiene polymers and graft copolymer | |
US2561951A (en) * | 1947-11-08 | 1951-07-24 | Harvel Res Corp | Polyethylene dispersion and method of making same |
US2656297A (en) * | 1949-04-02 | 1953-10-20 | B B Chem Co | Method of bonding a body of polyethylene to a surface and adhesives used therefor |
US2744085A (en) * | 1953-09-15 | 1956-05-01 | Du Pont | Process of making dispersions of polymers |
US2753287A (en) * | 1953-09-18 | 1956-07-03 | Millville Mfg Company | Organic dispersion type adhesives, their preparation and application |
US2888442A (en) * | 1954-04-09 | 1959-05-26 | Phillips Petroleum Co | New polymers from conjugated dienes and polyvinyl compounds prepared in the presence of mercaptans |
US2843561A (en) * | 1955-03-29 | 1958-07-15 | Dow Chemical Co | Compositions of interpolymerized vinyl aromatic hydrocarbons, acrylic acid esters and rubbery butadiene-styrene copolymers and method of making same |
US2820773A (en) * | 1955-08-01 | 1958-01-21 | Us Rubber Co | Method of preparing rubber-and-resin compositions |
US2946702A (en) * | 1956-08-31 | 1960-07-26 | American Marietta Co | High solids vinyl dispersions |
US2966474A (en) * | 1956-12-08 | 1960-12-27 | Glanzstoff Ag | Method of preparing stable polyolefin dispersion |
US3095388A (en) * | 1957-05-27 | 1963-06-25 | Ici Ltd | Dispersion polymerisation of an acrylate in the presence of a rubber and a non-polar organic solvent and product obtained |
-
0
- NL NL264369D patent/NL264369A/xx unknown
- NL NL264411D patent/NL264411A/xx unknown
- BE BE603339D patent/BE603339A/xx unknown
-
1961
- 1961-05-01 US US10650161 patent/US3257340A/en not_active Expired - Lifetime
- 1961-05-01 US US10652861 patent/US3257341A/en not_active Expired - Lifetime
- 1961-05-02 LU LU40084D patent/LU40084A1/xx unknown
- 1961-05-03 LU LU40085D patent/LU40085A1/xx unknown
- 1961-05-04 CH CH525661A patent/CH402410A/de unknown
-
1965
- 1965-12-30 MY MY171/65A patent/MY6500171A/xx unknown
- 1965-12-30 MY MY165/65A patent/MY6500165A/xx unknown
Also Published As
Publication number | Publication date |
---|---|
MY6500165A (en) | 1965-12-31 |
MY6500171A (en) | 1965-12-31 |
BE603339A (en, 2012) | 1900-01-01 |
LU40084A1 (en, 2012) | 1961-07-03 |
US3257341A (en) | 1966-06-21 |
LU40085A1 (en, 2012) | 1961-07-03 |
NL264411A (en, 2012) | 1900-01-01 |
NL264369A (en, 2012) | 1900-01-01 |
US3257340A (en) | 1966-06-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE1911882C3 (en, 2012) | ||
DE1520119C3 (de) | Verfahren zur Herstellung einer stabilen Dispersion eines Additionspolymeren in einer organischen Flüssigkeit | |
DE4105134C1 (en, 2012) | ||
DE2225578A1 (de) | Formmasse zur herstellung lichtstreuender formkoerper | |
EP0033365B1 (de) | Verfahren zur Herstellung schlagzäher Formmassen | |
DE3888520T2 (de) | Hoch vernetzte Polymerteilchen und Verfahren zur Herstellung derselben. | |
CH673463A5 (en, 2012) | ||
CH402410A (de) | Verfahren zur Herstellung einer Polymer-Dispersion | |
DE2032953B2 (de) | Verfahren zur herstellung perlfoermiger polymerisate der acrylsaeure und verwendung dieser polyacrylsaeuren | |
DE4340648A1 (de) | Wäßrige Polymerdispersionen als Bindemittel für blockfeste, kratzfeste und chemikalienbeständige Beschichtungen | |
EP0671420A2 (de) | Schutzkolloid-stabilisierte Polyacrylat-Dispersionen | |
DE4440219A1 (de) | Verfahren zur Herstellung von Copolymerisaten aus Alkylmethacrylat, Vinylaromaten und Maleinsäureanhydrid | |
EP0073296A1 (de) | Verfahren zur Herstellung von Acrylkunststoffdispersionen | |
DE1093992B (de) | Verfahren zur Herstellung eines in einer organischen Fluessigkeit dispergierten Polymerisats | |
DE1720551A1 (de) | Bitumenmischung | |
DE1269360B (de) | Verfahren zur Herstellung von thermoplastisch-elastischen Formmassen | |
AT232275B (de) | Verfahren zur Herstellung einer frei fließfähigen Dispersion eines polaren synthetischen Polymers in einer relativ nichtpolaren Flüssigkeit | |
DE1720897B2 (de) | Verfahren zum Polymerisieren von äthylenisch ungesättigten Monomeren in wäßriger Emulsion | |
EP0095627B1 (de) | Wärmehärtbare Acrylatbindemittel und Verfahren zu ihrer Herstellung | |
EP0320930B1 (de) | Verfahren zur Emulsionspolymerisation von Pfropfcopolymeren | |
DE3782320T2 (de) | Nicht-waesserige polymer-dispersion und verfahren zu ihrer herstellung. | |
AT237289B (de) | Verfahren zur Herstellung einer frei fließfähigen Dispersion eines polaren synthetischen Polymers in einer relativ nichtpolaren Flüssigkeit | |
DE1595672C3 (de) | Verfahren zur Herstellung von mit Monoolefinen modifizierten Pfropfpolymerisaten des Vinylchlorids auf Äthylen-Vinylacetat-Copolymerisate | |
DE882593C (de) | Verfahren zur Herstellung von Zahnersatz | |
DE1954434C3 (de) | Verwendung eines wäßrigen Latex eines Additionspolymerisats zum Überziehen eines Substrats |