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 PDF

Info

Publication number: NO309725B1
Authority: NO; Norway
Prior art keywords: chemical composition; meth; acrylate; copolymer; protective colloid
Prior art date: 1995-01-26

Application number

NO960299A

Other languages

English (en)

Norwegian (no)

Other versions

NO960299D0 (no

NO960299L (no

Inventor

Robert Koelliker

Harald Bachler

Original Assignee

Nat Starch Chem Invest

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.)

1995-01-26

Filing date

1996-01-25

Publication date

2001-03-19

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=7752392&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO309725(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1996-01-25 Application filed by Nat Starch Chem Invest filed Critical Nat Starch Chem Invest

1996-01-25 Publication of NO960299D0 publication Critical patent/NO960299D0/no

1996-07-29 Publication of NO960299L publication Critical patent/NO960299L/no

2001-03-19 Publication of NO309725B1 publication Critical patent/NO309725B1/no

Links

239000000203 mixture Substances 0.000 title claims abstract description 66
239000000126 substance Substances 0.000 title claims abstract description 46
238000000034 method Methods 0.000 title claims abstract description 44
230000001681 protective effect Effects 0.000 title claims abstract description 43
239000000084 colloidal system Substances 0.000 title claims abstract description 39
229920001577 copolymer Polymers 0.000 title claims abstract description 24
239000012736 aqueous medium Substances 0.000 title claims abstract description 10
230000008569 process Effects 0.000 title claims description 10
238000002360 preparation method Methods 0.000 title description 2
239000000178 monomer Substances 0.000 claims abstract description 70
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims abstract description 37
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
239000000654 additive Substances 0.000 claims abstract description 8
125000000468 ketone group Chemical group 0.000 claims abstract description 8
239000004815 dispersion polymer Substances 0.000 claims abstract description 7
125000003700 epoxy group Chemical group 0.000 claims abstract description 6
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 5
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims abstract 2
239000006185 dispersion Substances 0.000 claims description 54
229920002451 polyvinyl alcohol Polymers 0.000 claims description 30
239000004372 Polyvinyl alcohol Substances 0.000 claims description 29
238000006116 polymerization reaction Methods 0.000 claims description 27
150000002118 epoxides Chemical group 0.000 claims description 23
239000003999 initiator Substances 0.000 claims description 20
239000000843 powder Substances 0.000 claims description 20
-1 2-ethylhexyl Chemical group 0.000 claims description 18
239000002245 particle Substances 0.000 claims description 17
239000003995 emulsifying agent Substances 0.000 claims description 16
239000000853 adhesive Substances 0.000 claims description 13
230000001070 adhesive effect Effects 0.000 claims description 13
229920003023 plastic Polymers 0.000 claims description 11
239000004033 plastic Substances 0.000 claims description 11
239000004570 mortar (masonry) Substances 0.000 claims description 10
238000001694 spray drying Methods 0.000 claims description 10
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 7
239000004568 cement Substances 0.000 claims description 7
239000003973 paint Substances 0.000 claims description 7
229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 6
239000001267 polyvinylpyrrolidone Substances 0.000 claims description 6
235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 6
239000011230 binding agent Substances 0.000 claims description 5
229920000058 polyacrylate Polymers 0.000 claims description 5
239000008346 aqueous phase Substances 0.000 claims description 4
239000002612 dispersion medium Substances 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
230000007062 hydrolysis Effects 0.000 claims description 4
238000006460 hydrolysis reaction Methods 0.000 claims description 4
239000002131 composite material Substances 0.000 claims description 3
JJRUAPNVLBABCN-UHFFFAOYSA-N 2-(ethenoxymethyl)oxirane Chemical group C=COCC1CO1 JJRUAPNVLBABCN-UHFFFAOYSA-N 0.000 claims description 2
LSWYGACWGAICNM-UHFFFAOYSA-N 2-(prop-2-enoxymethyl)oxirane Chemical compound C=CCOCC1CO1 LSWYGACWGAICNM-UHFFFAOYSA-N 0.000 claims description 2
125000000129 anionic group Chemical group 0.000 claims description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
125000002091 cationic group Chemical group 0.000 claims description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
239000003365 glass fiber Substances 0.000 claims description 2
239000003292 glue Substances 0.000 claims description 2
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 2
239000008247 solid mixture Substances 0.000 claims description 2
239000002023 wood Substances 0.000 claims description 2
125000004185 ester group Chemical group 0.000 claims 1
239000012875 nonionic emulsifier Substances 0.000 claims 1
238000004519 manufacturing process Methods 0.000 abstract description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 25
238000006243 chemical reaction Methods 0.000 description 23
239000007787 solid Substances 0.000 description 13
150000003254 radicals Chemical class 0.000 description 10
150000001299 aldehydes Chemical class 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 8
239000000463 material Substances 0.000 description 7
229920000642 polymer Polymers 0.000 description 7
239000000047 product Substances 0.000 description 7
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
239000003638 chemical reducing agent Substances 0.000 description 6
CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 6
239000004908 Emulsion polymer Substances 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
239000011162 core material Substances 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
238000007720 emulsion polymerization reaction Methods 0.000 description 5
239000011257 shell material Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
238000003756 stirring Methods 0.000 description 5
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 4
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
150000001252 acrylic acid derivatives Chemical class 0.000 description 4
150000001875 compounds Chemical class 0.000 description 4
238000004132 cross linking Methods 0.000 description 4
239000011505 plaster Substances 0.000 description 4
239000011734 sodium Substances 0.000 description 4
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
230000008901 benefit Effects 0.000 description 3
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
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
235000014113 dietary fatty acids Nutrition 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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
230000006872 improvement Effects 0.000 description 3
239000002609 medium Substances 0.000 description 3
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
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001336 alkenes Chemical class 0.000 description 2
229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 2
150000008052 alkyl sulfonates Chemical class 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
239000012223 aqueous fraction Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000007853 buffer solution Substances 0.000 description 2
AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 2
239000000920 calcium hydroxide Substances 0.000 description 2
229910001861 calcium hydroxide Inorganic materials 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
235000019439 ethyl acetate Nutrition 0.000 description 2
239000000284 extract Substances 0.000 description 2
238000011049 filling Methods 0.000 description 2
230000009477 glass transition Effects 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
239000004816 latex Substances 0.000 description 2
229920000126 latex Polymers 0.000 description 2
239000007788 liquid Substances 0.000 description 2
150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
150000002825 nitriles Chemical class 0.000 description 2
229920000847 nonoxynol Polymers 0.000 description 2
239000000049 pigment Substances 0.000 description 2
239000004848 polyfunctional curative Substances 0.000 description 2
239000011591 potassium Substances 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
235000017557 sodium bicarbonate Nutrition 0.000 description 2
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
PAOHAQSLJSMLAT-UHFFFAOYSA-N 1-butylperoxybutane Chemical compound CCCCOOCCCC PAOHAQSLJSMLAT-UHFFFAOYSA-N 0.000 description 1
LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 1
CCNDGKOREYKPJK-UHFFFAOYSA-N 1-hydroperoxy-2,3-di(propan-2-yl)benzene Chemical compound CC(C)C1=CC=CC(OO)=C1C(C)C CCNDGKOREYKPJK-UHFFFAOYSA-N 0.000 description 1
238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
BJELTSYBAHKXRW-UHFFFAOYSA-N 2,4,6-triallyloxy-1,3,5-triazine Chemical compound C=CCOC1=NC(OCC=C)=NC(OCC=C)=N1 BJELTSYBAHKXRW-UHFFFAOYSA-N 0.000 description 1
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
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
LIZVXGBYTGTTTI-UHFFFAOYSA-N 2-[(4-methylphenyl)sulfonylamino]-2-phenylacetic acid Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC(C(O)=O)C1=CC=CC=C1 LIZVXGBYTGTTTI-UHFFFAOYSA-N 0.000 description 1
KIFPIAKBYOIOCS-UHFFFAOYSA-N 2-methyl-2-(trioxidanyl)propane Chemical compound CC(C)(C)OOO KIFPIAKBYOIOCS-UHFFFAOYSA-N 0.000 description 1
FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 1
ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
229920002126 Acrylic acid copolymer Polymers 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
239000004641 Diallyl-phthalate Substances 0.000 description 1
PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
229920000881 Modified starch Polymers 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
239000011398 Portland cement Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical class C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
LXEKPEMOWBOYRF-UHFFFAOYSA-N [2-[(1-azaniumyl-1-imino-2-methylpropan-2-yl)diazenyl]-2-methylpropanimidoyl]azanium;dichloride Chemical compound Cl.Cl.NC(=N)C(C)(C)N=NC(C)(C)C(N)=N LXEKPEMOWBOYRF-UHFFFAOYSA-N 0.000 description 1
239000012190 activator Substances 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
125000005234 alkyl aluminium group Chemical group 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
125000004390 alkyl sulfonyl group Chemical group 0.000 description 1
125000005233 alkylalcohol group Chemical group 0.000 description 1
229940009827 aluminum acetate Drugs 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
229960005070 ascorbic acid Drugs 0.000 description 1
235000010323 ascorbic acid Nutrition 0.000 description 1
239000011668 ascorbic acid Substances 0.000 description 1
238000010923 batch production Methods 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
239000002981 blocking agent Substances 0.000 description 1
CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
230000008859 change Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
239000000470 constituent Substances 0.000 description 1
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
239000000945 filler Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
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)

NO960299A 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 NO309725B1 (no)

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 (fr)
EP (1)	EP0723975B1 (fr)
JP (1)	JP2831317B2 (fr)
AT (1)	ATE179993T1 (fr)
CA (1)	CA2168157C (fr)
DE (2)	DE19502435A1 (fr)
DK (1)	DK0723975T3 (fr)
NO (1)	NO309725B1 (fr)
TW (1)	TW432077B (fr)

Families Citing this family (37)

* Cited by examiner, † Cited by third party
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
JP2003518174A (ja)	1999-12-21	2003-06-03	オムノヴアソリユーシヨンズインコーポレーテツド	ポリビニルアルコールコポリマー組成物
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
KR20070026365A (ko) *	2004-06-09	2007-03-08	가부시키가이샤 구라레	수성 분산액, 조성물 및 종이용 코팅제
US8524822B2 (en)	2005-01-11	2013-09-03	W. R. Grace & Co.—Conn.	Vapor permeable liquid-applied membrane
EP1767506A1 (fr)	2005-09-27	2007-03-28	Elotex AG	Poudres redispersables dans l'eau, procédé de production de lesdites poudres et leur utilisation
EP1958985B1 (fr) *	2005-11-24	2010-04-21	The Nippon Synthetic Chemical Industry Co., Ltd.	Poudre de resine re-emulsifiable, emulsion aqueuse et composition adhesive l'utilisant
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
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 (fr)	2010-07-16	2012-01-19	Parexlanko	Composition sèche redispersable de couche de finition polymère
DE102011076407A1 (de)	2011-05-24	2012-11-29	Wacker Chemie Ag	Verfahren zur Herstellung von Schutzkolloid-stabilisierten Polymerisaten
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
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
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
WO2014055494A1 (fr)	2012-10-03	2014-04-10	Dow Global Technologies Llc	Particules de polymère multicouche re-dispersibles (rdp) à enveloppe de résine époxy soluble dans les alkalis (asr) présentant une stabilité de conservation améliorée
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
WO2020173547A1 (fr)	2019-02-26	2020-09-03	Wacker Chemie Ag	Compositions pulvérulentes polymères réticulables, redispersibles dans l'eau

Family Cites Families (38)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE346728C (de) *		1922-01-06	Willy Horn Dipl Ing	Bremse fuer eine Treibscheibe fuer Foerdermaschinen mit elektromagnetischer Festhaltung des Foerderseils
US2773050A (en) *	1952-04-30	1956-12-04	Eastman Kodak Co	Water vapor permeable compositions and articles containing a polyacrylic ester and polyvinyl alcohol
DE1072813B (de) *	1958-08-01	1960-01-07	Wacker-Chemie G.m.b.H., München	Verfahren zur Herstellung stabiler wäßriger Polymerisat-Dispersionen aus Vinylestern
DE1144152B (de) *	1961-02-07	1963-02-21	Licentia Gmbh	Scherkopf fuer Trockenrasiergeraete
US3758635A (en) *	1971-08-16	1973-09-11	Ford Motor Co	Flow control agents powdered coating compositions of unsaturated glycidyl copolymers with
US4009131A (en) *	1972-01-17	1977-02-22	The Lubrizol Corporation	Powder coating compositions and metal objects coated therewith
GB1435821A (en) *	1972-09-26	1976-05-19	Dainippon Toryo Kk	Polymer particles and process for preparing the same
JPS515871B2 (fr) *	1973-01-19	1976-02-23	Nippon Synthetic Chem Ind
CA1045279A (fr) *	1973-09-06	1978-12-26	Elaine C. Siwiec	Produit de revetement en poudre
US3991132A (en) *	1973-09-06	1976-11-09	Ford Motor Company	Powder paint with epoxy and amide copolymer with anhydrides and hydroxy acids
US4374954A (en) *	1973-09-06	1983-02-22	Ford Motor Company	Powder paint with epoxy and hydroxy copolymer and anhydride
US3959405A (en) *	1973-12-19	1976-05-25	Ford Motor Company	Powder coating compositions comprising a blend of coreactive polymers - III
DE2451772A1 (de) *	1974-10-31	1976-05-13	Hoechst Ag	Verfahren zum herstellen von kunststoff-dispersionen
JPS6014964B2 (ja) *	1978-04-05	1985-04-17	株式会社日立製作所	多管式熱交換器
JPS5655408A (en) *	1979-10-13	1981-05-16	Daicel Chem Ind Ltd	Pigmented aqueous polymer emulsion composition
DE3031531A1 (de) *	1980-08-21	1982-04-08	Robert Bosch Gmbh, 7000 Stuttgart	Sensoranordnung
DE3111602A1 (de) *	1981-03-24	1982-10-07	Wacker-Chemie GmbH, 8000 München	Copolymerisate erhoehter wasserfestigkeit, verfahren zu ihrer herstellung und ihre verwendung
DE3143071A1 (de) *	1981-10-30	1983-05-11	Basf Ag, 6700 Ludwigshafen	Verfahren zum herstellen von blockfesten, in wasser redispergierbaren polymerisat-pulvern durch verspruehen von waessrigen polymerisat-dispersionen
JPS58162611A (ja) *	1982-03-23	1983-09-27	Daicel Chem Ind Ltd	アクリル系重合体エマルジヨンの製法
EP0095263B1 (fr) *	1982-05-20	1987-07-22	Imperial Chemical Industries Plc	Procédé de préparation de dispersions aqueuses stabiliseés stériquement non chargeés de polymères
JPH0665682B2 (ja) *	1985-02-01	1994-08-24	関西ペイント株式会社	重合体粒子の安定な水性分散液の製造方法
US4670505A (en) *	1985-08-23	1987-06-02	Hercules Incorporated	Polyacrylate dispersions
US4774291A (en) *	1985-12-26	1988-09-27	Denki Kagaku Kogyo Kabushiki Kaisha	Polymer composition
JPH078538B2 (ja) *	1986-12-29	1995-02-01	川鉄鋼板株式会社	ふつ素樹脂フイルムラミネ−ト板の製造方法
US4816501A (en) *	1987-05-07	1989-03-28	Denki Kagaku Kogyo Kabushiki Kaisha	Heat-sensitive color developable composition
DE3820154A1 (de) *	1988-06-14	1989-12-21	Basf Ag	Waessrige dispersionen von copolymerisaten, die epoxidgruppen enthalten und deren anwendung
US5244737A (en) *	1989-03-23	1993-09-14	Ici Australia Operations Proprietary Limited	Addition polymer particles
JPH03250003A (ja) *	1990-02-28	1991-11-07	Oji Kako Kk	水溶性樹脂エマルジョンおよびその製法
DE4030638A1 (de) *	1990-09-27	1992-04-02	Wacker Chemie Gmbh	Dispersionspulverzusammensetzung
US5362803A (en) *	1990-12-07	1994-11-08	Rohm And Haas Company	Polymeric blends of polyvinyl alcohol copolymers with copolymers of unsaturated monomers
US5405879A (en) *	1991-04-05	1995-04-11	Nippon Carbide Kogyo Kabushiki Kaisha	Aqueous dispersion of acrylic polymer
DE4134672A1 (de) *	1991-10-19	1993-04-22	Huels Chemische Werke Ag	Verfahren zur herstellung von schutzkolloidstabilisierten, emulgatorfreien, waessrigen kunststoffdispersionen
US5354800A (en) *	1991-10-31	1994-10-11	Takeda Chemical Industries, Ltd.	Production of copolymer latices
JP3342883B2 (ja) *	1991-11-19	2002-11-11	クラリアントインターナショナルリミテッド	再乳化性合成樹脂エマルジョン粉末組成物およびその製造方法
JP3085490B2 (ja) *	1992-05-07	2000-09-11	富士写真フイルム株式会社	写真フイルムパトローネ及びカメラ並びにカメラの磁気ヘッドクリーニング方法
US5252704A (en) *	1992-06-05	1993-10-12	Air Products And Chemicals, Inc.	Redispersible polymer powders using polyvinyl pyrrolidone as a dispersing aid
CA2110448A1 (fr) *	1992-12-08	1994-06-09	Helen H.Y. Pak-Harvey	Poudre acrylique de polymere redispersable, pour compositions cimentaires
DE4321070A1 (de) *	1993-06-24	1995-01-05	Wacker Chemie Gmbh	Redispergierbare Dispersionspulverzusammensetzung

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 AT AT96100581T patent/ATE179993T1/de not_active IP Right Cessation
- 1996-01-16 DE DE69602384T patent/DE69602384T2/de not_active Expired - Lifetime
- 1996-01-16 EP EP96100581A patent/EP0723975B1/fr 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/fr 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
US5959029A (en)	1999-09-28
JP2831317B2 (ja)	1998-12-02
EP0723975A1 (fr)	1996-07-31
DK0723975T3 (da)	1999-11-15
ATE179993T1 (de)	1999-05-15
NO960299D0 (no)	1996-01-25
CA2168157C (fr)	2001-02-27
JPH08239539A (ja)	1996-09-17
DE69602384D1 (de)	1999-06-17
DE69602384T2 (de)	2000-01-13
CA2168157A1 (fr)	1996-07-27
DE19502435A1 (de)	1996-08-01
NO960299L (no)	1996-07-29
TW432077B (en)	2001-05-01
EP0723975B1 (fr)	1999-05-12

Legal Events

Date	Code	Title	Description
2003-09-01	MM1K	Lapsed by not paying the annual fees	Free format text: LAPSED IN JULY 2003

Publication	Publication Date	Title
EP0723975B1 (fr)	1999-05-12	Composition chimique redispersable dans un milieu aqueux contenant un copolymère et un colloide protecteur, sa dispersion aqueuse de polymère, procédé de sa production et son utilisation
JP3697157B2 (ja)	2005-09-21	不均質形態を有するラテックス粒子の水性分散液の製造方法、この方法によって得られるラテックス粒子、分散液、再分散性粉末、
CA2337855C (fr)	2008-10-07	Poudre redispersible, sa dispersion aqueuse, son procede de preparation et ses utilisations
JP3418406B2 (ja)	2003-06-23	乾燥モルタル混合物
TWI391407B (zh)	2013-04-01	連續聚合方法
JP3574796B2 (ja)	2004-10-06	ポリビニルアルコールで安定化されたポリマーの製法およびその方法生成物の使用
US6316568B1 (en)	2001-11-13	Crosslinkable protective colloids for use in the polymerization of unsaturated monomers
US6534177B2 (en)	2003-03-18	Crosslinkable polymer composition
JPH09118721A (ja)	1997-05-06	不均一な酢酸ビニル／エチレン分散物
JP3692113B2 (ja)	2005-09-07	連続的な乳化重合により保護コロイドで安定化されたポリマーの製法
US6063865A (en)	2000-05-16	Crosslinkable powder composition which is redispersible in water
CZ20001078A3 (cs)	2000-07-12	Způsob výroby polymerů stabilizovaných ochranným koloidem
AU753348B2 (en)	2002-10-17	Latex particles based on a vinyl acetate-ethylene copolymerizate, processes for the production thereof and the use thereof
US9156977B2 (en)	2015-10-13	Process for producing protective colloid-stabilized polymers
US6605663B1 (en)	2003-08-12	Process for preparing polyvinyl alcohol-stabilized polymers
US6590022B1 (en)	2003-07-08	Process for preparing protective-colloid-stabilized vinylaromatic-1,3-diene copolymers
US6228937B1 (en)	2001-05-08	Crosslinkable powder composition which is redispersible in water
PL192455B1 (pl)	2006-10-31	Sposób wytwarzania stabilizowanych koloidami ochronnymi wodnych dyspersji polimerów oraz zastosowanie stablizowanych koloidami ochronnymi wodnych dyspersji polimerów
US20030040558A1 (en)	2003-02-27	High solids ethylene-vinyl acetate latex
US6235843B1 (en)	2001-05-22	Method for producing cross-linkable redispersible powders containing isocyanate groups