NO309725B1 - Kjemisk sammensetning som er redispergerbar i vandig medium, inneholdende en kopolymer og et beskyttende kolloid, fremgangsmåte for dens fremstilling og anvendelse derav - Google Patents
Kjemisk sammensetning som er redispergerbar i vandig medium, inneholdende en kopolymer og et beskyttende kolloid, fremgangsmåte for dens fremstilling og anvendelse derav Download PDFInfo
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- NO309725B1 NO309725B1 NO960299A NO960299A NO309725B1 NO 309725 B1 NO309725 B1 NO 309725B1 NO 960299 A NO960299 A NO 960299A NO 960299 A NO960299 A NO 960299A NO 309725 B1 NO309725 B1 NO 309725B1
- Authority
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- Norway
- Prior art keywords
- chemical composition
- meth
- acrylate
- copolymer
- protective colloid
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 66
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- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 35
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 21
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- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims abstract 2
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
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- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
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- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 3
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- 125000005385 peroxodisulfate group Chemical group 0.000 description 3
- 229920002689 polyvinyl acetate Polymers 0.000 description 3
- XWGJFPHUCFXLBL-UHFFFAOYSA-M rongalite Chemical compound [Na+].OCS([O-])=O XWGJFPHUCFXLBL-UHFFFAOYSA-M 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 150000003440 styrenes Chemical class 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid group Chemical group S(O)(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 3
- 238000010557 suspension polymerization reaction Methods 0.000 description 3
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
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- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
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- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
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- 238000001816 cooling Methods 0.000 description 1
- 125000006165 cyclic alkyl group Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- MAWOHFOSAIXURX-UHFFFAOYSA-N cyclopentylcyclopentane Chemical group C1CCCC1C1CCCC1 MAWOHFOSAIXURX-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000006735 epoxidation reaction Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 230000007717 exclusion Effects 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
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- 238000001914 filtration Methods 0.000 description 1
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- 229920000159 gelatin Polymers 0.000 description 1
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- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 150000004676 glycans Chemical class 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 125000001400 nonyl 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])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 150000002898 organic sulfur compounds Chemical class 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000011164 primary particle Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- VYGBQXDNOUHIBZ-UHFFFAOYSA-L sodium formaldehyde sulphoxylate Chemical compound [Na+].[Na+].O=C.[O-]S[O-] VYGBQXDNOUHIBZ-UHFFFAOYSA-L 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052572 stoneware Inorganic materials 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 150000003623 transition metal compounds Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/2641—Polyacrylates; Polymethacrylates
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B24/00—Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
- C04B24/24—Macromolecular compounds
- C04B24/26—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C04B24/2676—Polystyrenes
-
- 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
- C08F212/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring
- C08F212/02—Monomers containing only one unsaturated aliphatic radical
- C08F212/04—Monomers containing only one unsaturated aliphatic radical containing one ring
- C08F212/06—Hydrocarbons
- C08F212/08—Styrene
-
- 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
- C08F220/00—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
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
-
- 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
- C08F261/00—Macromolecular compounds obtained by polymerising monomers on to polymers of oxygen-containing monomers as defined in group C08F16/00
- C08F261/02—Macromolecular compounds obtained by polymerising monomers on to polymers of oxygen-containing monomers as defined in group C08F16/00 on to polymers of unsaturated alcohols
- C08F261/04—Macromolecular compounds obtained by polymerising monomers on to polymers of oxygen-containing monomers as defined in group C08F16/00 on to polymers of unsaturated alcohols on to polymers of vinyl alcohol
-
- 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
- C08F265/00—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00
- C08F265/04—Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group C08F20/00 on to polymers of esters
-
- 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
- C08F271/00—Macromolecular compounds obtained by polymerising monomers on to polymers of nitrogen-containing monomers as defined in group C08F26/00
- C08F271/02—Macromolecular compounds obtained by polymerising monomers on to polymers of nitrogen-containing monomers as defined in group C08F26/00 on to polymers of monomers containing heterocyclic nitrogen
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2103/00—Function or property of ingredients for mortars, concrete or artificial stone
- C04B2103/0045—Polymers chosen for their physico-chemical characteristics
- C04B2103/0057—Polymers chosen for their physico-chemical characteristics added as redispersable powders
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Paints Or Removers (AREA)
- Polymerisation Methods In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Management, Administration, Business Operations System, And Electronic Commerce (AREA)
- Traffic Control Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19502435A DE19502435A1 (de) | 1995-01-26 | 1995-01-26 | Chemische Zusammensetzung mit einem Gehalt an a) einem Copolymer auf Basis von Styrol und/oder Alkyl(meth)acrylat sowie mindestens eines weiteren Comonomers und b) an einem Schutzkolloid, deren wäßrige Polymerdispersion, Verfahren zu ihrer Herstellung und ihre Verwendung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO960299D0 NO960299D0 (no) | 1996-01-25 |
| NO960299L NO960299L (no) | 1996-07-29 |
| NO309725B1 true NO309725B1 (no) | 2001-03-19 |
Family
ID=7752392
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO960299A NO309725B1 (no) | 1995-01-26 | 1996-01-25 | Kjemisk sammensetning som er redispergerbar i vandig medium, inneholdende en kopolymer og et beskyttende kolloid, fremgangsmåte for dens fremstilling og anvendelse derav |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5959029A (de) |
| EP (1) | EP0723975B1 (de) |
| JP (1) | JP2831317B2 (de) |
| AT (1) | ATE179993T1 (de) |
| CA (1) | CA2168157C (de) |
| DE (2) | DE19502435A1 (de) |
| DK (1) | DK0723975T3 (de) |
| NO (1) | NO309725B1 (de) |
| TW (1) | TW432077B (de) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5741871A (en) * | 1996-06-14 | 1998-04-21 | Air Products And Chemicals, Inc. | Acrylic emulsions prepared in the presence of fully hydrolyzed poly (vinyl alcohol) |
| DE19710381A1 (de) * | 1997-03-13 | 1998-09-17 | Buna Sow Leuna Olefinverb Gmbh | Redispergierbare Dispersionspulver auf Basis von Polyacrylaten |
| US5753036A (en) * | 1997-04-21 | 1998-05-19 | Air Products And Chemicals, Inc. | Poly(vinyl alcohol) stabilized acrylic polymer modified hydraulic cement systems |
| DE19733104A1 (de) * | 1997-07-31 | 1999-02-04 | Wacker Chemie Gmbh | Vernetzbare, in Wasser redispergierbare Pulverzusammensetzung |
| DE19837856A1 (de) | 1998-08-20 | 2000-02-24 | Wacker Chemie Gmbh | Schutzkolloidstabilisierte Polymer-Zusammensetzungen |
| DE19850658A1 (de) * | 1998-11-03 | 2000-06-15 | Elotex Ag Sempach Station | Redispergierbares Material, Verfahren zu dessen Herstellung und dessen Verwendung sowie ein wäßriges System, enthaltend das redispergierbare Material |
| DE19853489A1 (de) * | 1998-11-19 | 2000-05-25 | Wacker Chemie Gmbh | Verwendung von Schutzkolloid-stabilisierten Vinylaromat-1,3-Dien-Mischpolymerisaten in Baukleber-Rezepturen |
| DE19949593A1 (de) | 1999-10-14 | 2001-04-19 | Basf Ag | Thermisch härtbares polymeres Bindemittel in Pulverform |
| ATE321079T1 (de) | 1999-12-21 | 2006-04-15 | Omnova Solutions Inc | Polyvinylalkoholcopolymerzusammensetzung |
| DE10040825A1 (de) † | 2000-08-21 | 2002-03-07 | Basf Ag | Verwendung von Ammoniak-freien Polymerdispersionen als Zusatz in Baumaterialien auf Basis hydraulischer Bindemittel |
| DE10049127C2 (de) * | 2000-10-02 | 2003-02-20 | Clariant Gmbh | Redispergierbare Dispersionspulver-Zusammensetzung, Verfahren zu deren Herstellung sowie deren Verwendung |
| DE10132614A1 (de) | 2001-07-05 | 2003-01-16 | Polymerlatex Gmbh & Co Kg | Verfahren zur Herstellung von schutzkolloidstabilisierten, emulgatorfreien, wässrigen Dispersionen |
| DE10226088A1 (de) * | 2002-06-12 | 2004-03-04 | Elotex Ag | Additiv für hydraulisch abbindende Systeme, die hydraulisch abbindenden Mischungen sowie deren Verwendung |
| US6861475B2 (en) * | 2002-10-16 | 2005-03-01 | Rohm And Haas Company | Smooth, flexible powder coatings |
| DE10253045A1 (de) * | 2002-11-14 | 2004-06-03 | Wacker Polymer Systems Gmbh & Co. Kg | In Wasser redispergierbare Polymerpulver-Zusammensetzungen mit abbindebeschleunigender Wirkung |
| US20040143038A1 (en) * | 2003-01-16 | 2004-07-22 | Thomas Aberle | Age-stable composition having a polysaccharide |
| EP1754751A4 (de) * | 2004-06-09 | 2007-09-05 | Kuraray Co Ltd Kurashiki Plant | Wässrige dispersion, zusammensetzung und beschichtungsmittel für papier |
| US8524822B2 (en) | 2005-01-11 | 2013-09-03 | W. R. Grace & Co.—Conn. | Vapor permeable liquid-applied membrane |
| EP1767506A1 (de) | 2005-09-27 | 2007-03-28 | Elotex AG | In Wasser redispergierbares Pulver, Herstellverfahren und Verwendung |
| JP5398115B2 (ja) * | 2005-11-24 | 2014-01-29 | 日本合成化学工業株式会社 | 再乳化性樹脂粉末、水性エマルジョン、及びそれを用いた接着剤組成物 |
| DE602006013874D1 (de) * | 2005-11-24 | 2010-06-02 | Nippon Synthetic Chem Ind | Wässrige emulsion und klebstofffzusammensetzung |
| KR100830909B1 (ko) * | 2007-04-27 | 2008-05-22 | (주)영우켐텍 | 아크릴산 에스테르 공중합체 조성물 및 재분산성 분말 |
| JP4489799B2 (ja) | 2007-08-27 | 2010-06-23 | セイコーエプソン株式会社 | 電気泳動表示装置用シート、その製造方法およびその用途 |
| JP4410815B2 (ja) | 2007-09-04 | 2010-02-03 | セイコーエプソン株式会社 | 電気泳動表示装置用塗工液組成物、電気泳動表示装置用シート、その製造方法およびその用途 |
| DE102009000537A1 (de) | 2009-02-02 | 2010-08-05 | Wacker Chemie Ag | Vernetzbare, in Wasser redispergierbare Polymerpulver-Zusammensetzung |
| US8674039B2 (en) | 2009-02-02 | 2014-03-18 | Wacker Chemie Ag | Crosslinkable polymer powder composition which is redispersible in water |
| WO2012007057A1 (en) | 2010-07-16 | 2012-01-19 | Parexlanko | Redispersible dry composition of polymer finish |
| DE102011076407A1 (de) | 2011-05-24 | 2012-11-29 | Wacker Chemie Ag | Verfahren zur Herstellung von Schutzkolloid-stabilisierten Polymerisaten |
| JP5385424B2 (ja) * | 2011-06-23 | 2014-01-08 | ダウ グローバル テクノロジーズ エルエルシー | 界面反応による再分散可能なエポキシ粉体 |
| BR112013031811B1 (pt) | 2011-06-23 | 2020-05-19 | Dow Global Technologies Llc | pó de polímero de epóxi redispersável em água, método para preparar o pó de polímero de epóxi dispersável em água, e, dispersão do pó de polímero de epóxi redispersável em água |
| JP5479530B2 (ja) * | 2011-06-23 | 2014-04-23 | ダウ グローバル テクノロジーズ エルエルシー | 再分散可能なエポキシ粉体 |
| CN104822734B (zh) | 2012-10-03 | 2017-06-20 | 陶氏环球技术有限公司 | 展现改进的存放稳定性的碱溶性树脂(asr)壳环氧树脂rdp |
| DE102013219325A1 (de) | 2013-09-25 | 2015-03-26 | Wacker Chemie Ag | Verwendung von modifizierten wasserlöslichen Polymeren als Vernetzungshilfsmittel |
| RU2568440C1 (ru) * | 2014-10-21 | 2015-11-20 | Открытое акционерное общество "Казанский химический научно-исследовательский институт" | Водная стиролакриловая дисперсия и способ ее получения |
| JP6510855B2 (ja) * | 2015-03-30 | 2019-05-08 | 積水化学工業株式会社 | ポリビニルアルコールハイドロゲル粒子 |
| CN106590129A (zh) * | 2016-11-24 | 2017-04-26 | 安庆市凯瑞建材有限公司 | 一种外墙抗裂弹性腻子及其制备方法 |
| US12134692B2 (en) | 2019-02-26 | 2024-11-05 | Wacker Chemie Ag | Crosslinkable polymer-powder compositions redispersible in water |
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| DE1072813B (de) * | 1958-08-01 | 1960-01-07 | Wacker-Chemie G.m.b.H., München | Verfahren zur Herstellung stabiler wäßriger Polymerisat-Dispersionen aus Vinylestern |
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| US3991132A (en) * | 1973-09-06 | 1976-11-09 | Ford Motor Company | Powder paint with epoxy and amide copolymer with anhydrides and hydroxy acids |
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| US4670505A (en) * | 1985-08-23 | 1987-06-02 | Hercules Incorporated | Polyacrylate dispersions |
| EP0230030B1 (de) * | 1985-12-26 | 1993-05-19 | Denki Kagaku Kogyo Kabushiki Kaisha | Polymerzusammensetzung |
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-
1995
- 1995-01-26 DE DE19502435A patent/DE19502435A1/de not_active Withdrawn
-
1996
- 1996-01-16 DK DK96100581T patent/DK0723975T3/da active
- 1996-01-16 EP EP96100581A patent/EP0723975B1/de not_active Expired - Lifetime
- 1996-01-16 AT AT96100581T patent/ATE179993T1/de not_active IP Right Cessation
- 1996-01-16 DE DE69602384T patent/DE69602384T2/de not_active Expired - Lifetime
- 1996-01-25 JP JP8011240A patent/JP2831317B2/ja not_active Expired - Fee Related
- 1996-01-25 NO NO960299A patent/NO309725B1/no not_active IP Right Cessation
- 1996-01-26 CA CA002168157A patent/CA2168157C/en not_active Expired - Fee Related
- 1996-01-29 TW TW085101096A patent/TW432077B/zh not_active IP Right Cessation
-
1997
- 1997-08-18 US US08/912,801 patent/US5959029A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JP2831317B2 (ja) | 1998-12-02 |
| CA2168157C (en) | 2001-02-27 |
| NO960299D0 (no) | 1996-01-25 |
| EP0723975B1 (de) | 1999-05-12 |
| JPH08239539A (ja) | 1996-09-17 |
| ATE179993T1 (de) | 1999-05-15 |
| TW432077B (en) | 2001-05-01 |
| US5959029A (en) | 1999-09-28 |
| NO960299L (no) | 1996-07-29 |
| CA2168157A1 (en) | 1996-07-27 |
| DE19502435A1 (de) | 1996-08-01 |
| DE69602384D1 (de) | 1999-06-17 |
| DK0723975T3 (da) | 1999-11-15 |
| DE69602384T2 (de) | 2000-01-13 |
| EP0723975A1 (de) | 1996-07-31 |
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| MM1K | Lapsed by not paying the annual fees |
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