CS243466B2 - Method of film-forming polymer's particles aqueous dispersion preparation - Google Patents
Method of film-forming polymer's particles aqueous dispersion preparation Download PDFInfo
- Publication number
- CS243466B2 CS243466B2 CS815162A CS516281A CS243466B2 CS 243466 B2 CS243466 B2 CS 243466B2 CS 815162 A CS815162 A CS 815162A CS 516281 A CS516281 A CS 516281A CS 243466 B2 CS243466 B2 CS 243466B2
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- polymer
- dispersion
- dispersions
- surfactant
- water
- Prior art date
Links
- 239000006185 dispersion Substances 0.000 title claims abstract description 147
- 229920000642 polymer Polymers 0.000 title claims abstract description 121
- 238000000034 method Methods 0.000 title claims abstract description 42
- 239000002245 particle Substances 0.000 title claims abstract description 35
- 238000002360 preparation method Methods 0.000 title claims abstract description 17
- 239000004094 surface-active agent Substances 0.000 claims abstract description 47
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 44
- 239000000178 monomer Substances 0.000 claims abstract description 29
- 239000004014 plasticizer Substances 0.000 claims abstract description 19
- 238000011065 in-situ storage Methods 0.000 claims abstract description 17
- 238000000576 coating method Methods 0.000 claims description 39
- 239000011248 coating agent Substances 0.000 claims description 35
- 239000000203 mixture Substances 0.000 claims description 31
- 238000012360 testing method Methods 0.000 claims description 20
- 238000013112 stability test Methods 0.000 claims description 13
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 230000000977 initiatory effect Effects 0.000 claims description 9
- 230000000295 complement effect Effects 0.000 claims description 8
- 229920001577 copolymer Polymers 0.000 claims description 7
- 239000000758 substrate Substances 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- 239000003093 cationic surfactant Substances 0.000 claims description 5
- 239000000463 material Substances 0.000 claims description 3
- 230000014759 maintenance of location Effects 0.000 claims 1
- 229910052751 metal Inorganic materials 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 125000002091 cationic group Chemical group 0.000 abstract description 8
- 239000008199 coating composition Substances 0.000 abstract description 7
- 238000001962 electrophoresis Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 32
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 238000006116 polymerization reaction Methods 0.000 description 15
- 238000004132 cross linking Methods 0.000 description 13
- 239000008367 deionised water Substances 0.000 description 12
- 229910021641 deionized water Inorganic materials 0.000 description 12
- 239000003431 cross linking reagent Substances 0.000 description 11
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 10
- 239000000523 sample Substances 0.000 description 10
- 239000004971 Cross linker Substances 0.000 description 9
- 229920005989 resin Polymers 0.000 description 9
- 239000011347 resin Substances 0.000 description 9
- 239000003822 epoxy resin Substances 0.000 description 8
- 229920000647 polyepoxide Polymers 0.000 description 8
- 239000003153 chemical reaction reagent Substances 0.000 description 7
- 238000000151 deposition Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000003760 tallow Substances 0.000 description 7
- 230000008021 deposition Effects 0.000 description 6
- 239000010410 layer Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 229920001169 thermoplastic Polymers 0.000 description 6
- 229920003270 Cymel® Polymers 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 235000010323 ascorbic acid Nutrition 0.000 description 5
- 239000011668 ascorbic acid Substances 0.000 description 5
- 229960005070 ascorbic acid Drugs 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000012948 isocyanate Substances 0.000 description 5
- 150000002513 isocyanates Chemical class 0.000 description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 239000004416 thermosoftening plastic Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 238000010304 firing Methods 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
- 239000012470 diluted sample Substances 0.000 description 3
- 239000004815 dispersion polymer Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- -1 oleic acid primary amine acetates Chemical class 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000004645 polyester resin Substances 0.000 description 3
- 229920001225 polyester resin Polymers 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- 230000000087 stabilizing effect Effects 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000004070 electrodeposition Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000007888 film coating Substances 0.000 description 2
- 238000009501 film coating Methods 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 238000012544 monitoring process Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- GOLYTOVWWJCSJM-UHFFFAOYSA-N 3-butoxy-2-methylprop-2-enamide Chemical compound CCCCOC=C(C)C(N)=O GOLYTOVWWJCSJM-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- BTJIUGUIPKRLHP-UHFFFAOYSA-N 4-nitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1 BTJIUGUIPKRLHP-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical class NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 241000255632 Tabanus atratus Species 0.000 description 1
- IOYNQIMAUDJVEI-BMVIKAAMSA-N Tepraloxydim Chemical group C1C(=O)C(C(=N/OC\C=C\Cl)/CC)=C(O)CC1C1CCOCC1 IOYNQIMAUDJVEI-BMVIKAAMSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- ULQDZRWAROPNSH-UHFFFAOYSA-N acetic acid octane-1-thiol Chemical compound C(C)(=O)O.C(CCCCCCC)S ULQDZRWAROPNSH-UHFFFAOYSA-N 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 238000004581 coalescence Methods 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 239000000571 coke Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 125000001046 glycoluril group Chemical class [H]C12N(*)C(=O)N(*)C1([H])N(*)C(=O)N2* 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical group NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 150000004682 monohydrates Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical class CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000012149 noodles Nutrition 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- 230000005588 protonation Effects 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 235000010378 sodium ascorbate Nutrition 0.000 description 1
- PPASLZSBLFJQEF-RKJRWTFHSA-M sodium ascorbate Substances [Na+].OC[C@@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RKJRWTFHSA-M 0.000 description 1
- 229960005055 sodium ascorbate Drugs 0.000 description 1
- PPASLZSBLFJQEF-RXSVEWSESA-M sodium-L-ascorbate Chemical compound [Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-] PPASLZSBLFJQEF-RXSVEWSESA-M 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
-
- 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
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/22—Emulsion polymerisation
-
- 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
- C08F2/12—Polymerisation in non-solvents
- C08F2/16—Aqueous medium
- C08F2/20—Aqueous medium with the aid of macromolecular dispersing agents
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/02—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polycarbonates or saturated polyesters
-
- 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
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/10—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers containing more than one epoxy radical per molecule
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/44—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes for electrophoretic applications
- C09D5/4488—Cathodic paints
-
- 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
- Y10S524/901—Electrodepositable compositions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Materials Engineering (AREA)
- Molecular Biology (AREA)
- Paints Or Removers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Polymerisation Methods In General (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AUPE436080 | 1980-07-03 | ||
| AUPE930281 | 1981-06-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS516281A2 CS516281A2 (en) | 1985-08-31 |
| CS243466B2 true CS243466B2 (en) | 1986-06-12 |
Family
ID=25642392
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS815162A CS243466B2 (en) | 1980-07-03 | 1981-07-03 | Method of film-forming polymer's particles aqueous dispersion preparation |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US4373054A (h) |
| EP (1) | EP0055270B1 (h) |
| JP (1) | JPS57500880A (h) |
| KR (2) | KR840001789B1 (h) |
| AR (1) | AR226468A1 (h) |
| AT (1) | ATE16192T1 (h) |
| BE (1) | BE889512A (h) |
| BR (1) | BR8108666A (h) |
| CA (1) | CA1179436A (h) |
| CS (1) | CS243466B2 (h) |
| DE (1) | DE3172702D1 (h) |
| ES (1) | ES8203929A1 (h) |
| GR (1) | GR74918B (h) |
| IE (1) | IE51369B1 (h) |
| IN (1) | IN156779B (h) |
| IT (1) | IT1211074B (h) |
| MY (1) | MY8700282A (h) |
| NZ (1) | NZ197554A (h) |
| PH (1) | PH17170A (h) |
| PL (1) | PL131741B1 (h) |
| PT (1) | PT73317B (h) |
| RO (1) | RO83379B (h) |
| WO (1) | WO1982000148A1 (h) |
| YU (1) | YU165081A (h) |
| ZA (1) | ZA814473B (h) |
| ZW (1) | ZW15381A1 (h) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0094386B1 (en) * | 1981-06-29 | 1986-03-05 | Dulux Australia Ltd | Stable aqueous film-forming dispersions |
| EP0099179A3 (en) * | 1982-06-22 | 1987-01-21 | Imperial Chemical Industries Plc | Particulate dispersions |
| DE3476808D1 (en) * | 1983-08-11 | 1989-03-30 | Minnesota Mining & Mfg | Curable epoxy compositions and cured resins obtained therefrom |
| GB8321933D0 (en) * | 1983-08-15 | 1983-09-14 | Ici Plc | Coating compositions |
| GB8323241D0 (en) * | 1983-08-30 | 1983-09-28 | Ici Plc | Coating compositions |
| ZA854883B (en) * | 1984-08-27 | 1986-04-30 | Dulux Australia Ltd | Coating compositions |
| JP2686635B2 (ja) * | 1989-02-03 | 1997-12-08 | 神東塗料株式会社 | カチオン電着塗料組成物 |
| US5470906A (en) * | 1993-12-27 | 1995-11-28 | The Glidden Company | Odor free, air dry, decorative latex paints |
| US6221822B1 (en) | 1995-10-30 | 2001-04-24 | Tomah Products, Inc. | Detergent compositions having polyalkoxylated amine foam stabilizers |
| US5981458A (en) * | 1995-10-30 | 1999-11-09 | Crutcher; Terry | Detergent compositions having polyalkoxylated amine foam stabilizers |
| CN105874018B (zh) | 2013-11-18 | 2019-03-08 | 巴斯夫涂料有限公司 | 用于浸涂导电基底的包含溶解形式铋的水性涂料组合物 |
| EP3071658B1 (de) | 2013-11-18 | 2017-12-13 | BASF Coatings GmbH | Zweistufiges verfahren zur tauchlack-beschichtung elektrisch leitfähiger substrate unter verwendung einer bi(iii)-haltigen zusammensetzung |
| EP3071656B1 (de) | 2013-11-18 | 2019-05-22 | BASF Coatings GmbH | Wässrige beschichtungszusammensetzung zur tauchlack-beschichtung elektrisch leitfähiger substrate enthaltend bismut sowohl in gelöst als auch ungelöst vorliegender form |
| KR20160088376A (ko) | 2013-11-19 | 2016-07-25 | 바스프 코팅스 게엠베하 | 알루미늄 옥시드를 함유하는 전기 전도성 기판 딥코팅용 수성 코팅 조성물 |
| JP6285045B2 (ja) | 2013-11-19 | 2018-02-28 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 酸化マグネシウムを含む導電性基材のための水性ディップコーティング組成物 |
| JP6231217B2 (ja) | 2013-12-10 | 2017-11-15 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | ビスマスおよびリン含有アミンブロック化化合物を含む導電性基材のための水性ディップコーティング組成物 |
| KR20160102253A (ko) | 2013-12-20 | 2016-08-29 | 바스프 코팅스 게엠베하 | 수성 1 차 분산물, 그 제조 방법 및 용도 |
| JP6328267B2 (ja) | 2013-12-20 | 2018-05-23 | ビーエイエスエフ・コーティングス・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢＡＳＦ Ｃｏａｔｉｎｇｓ ＧｍｂＨ | 顔料および／またはフィラー含有製剤 |
| EP3083707B1 (de) | 2013-12-20 | 2019-02-06 | BASF Coatings GmbH | Wässrige primärdispersionen, verfahren zu ihrer herstellung und ihre verwendung |
| CN105874014B (zh) | 2013-12-20 | 2018-05-25 | 巴斯夫涂料有限公司 | 制备颜料糊的方法、水性电泳涂料、其用途、阳离子电泳涂覆方法和经涂覆的制品 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1421114A (en) * | 1972-07-14 | 1976-01-14 | Canadian Ind | Thermosettable synthetic addition polymers |
| DE2262610B2 (de) * | 1972-12-21 | 1980-01-03 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung schlagfester Styrolpolymerisate |
| DE2412266C3 (de) * | 1974-03-14 | 1981-12-10 | Röhm GmbH, 6100 Darmstadt | Wasserlösliche Polymerisate |
| DE2417712C2 (de) * | 1974-04-11 | 1983-04-21 | Röhm GmbH, 6100 Darmstadt | Verfahren zur Herstellung von Polymerisatsuspensionen |
| US3953386A (en) | 1974-07-02 | 1976-04-27 | E. I. Du Pont De Nemours And Company | Aqueous emulsions containing homogeneous particles of cellulosic ester/acrylic polymers |
| GB1513374A (en) * | 1974-07-16 | 1978-06-07 | Canadian Ind | Aqueous thermosettable coating compositions |
| GB1445238A (en) * | 1974-07-31 | 1976-08-04 | Okhtinskoe Naucho Proizv Ob Pl | Preparation of grafted copolymers |
| DE2454397C2 (de) * | 1974-11-16 | 1983-01-27 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung scherstabiler kationischer wäßriger Copolymerisat- Dispersionen |
| US4107234A (en) * | 1975-03-21 | 1978-08-15 | Uniroyal, Inc. | ABS Composition having improved impact strength and weather aging resistance and latex suspension process therefor |
| JPS5922722B2 (ja) * | 1975-09-12 | 1984-05-29 | 関西ペイント株式会社 | エマルジヨン組成物 |
| US4167499A (en) * | 1978-05-09 | 1979-09-11 | E. I. Du Pont De Nemours And Company | Graft copolymer useful in electrodeposition |
| GB2047273B (en) | 1979-02-27 | 1983-03-16 | Ici Ltd | Coating process |
-
1981
- 1981-06-25 AT AT81901791T patent/ATE16192T1/de active
- 1981-06-25 BR BR8108666A patent/BR8108666A/pt unknown
- 1981-06-25 JP JP56502148A patent/JPS57500880A/ja active Pending
- 1981-06-25 WO PCT/AU1981/000078 patent/WO1982000148A1/en not_active Ceased
- 1981-06-25 DE DE8181901791T patent/DE3172702D1/de not_active Expired
- 1981-06-25 EP EP81901791A patent/EP0055270B1/en not_active Expired
- 1981-06-29 NZ NZ197554A patent/NZ197554A/en unknown
- 1981-07-01 GR GR65407A patent/GR74918B/el unknown
- 1981-07-01 ZA ZA814473A patent/ZA814473B/xx unknown
- 1981-07-01 AR AR285947A patent/AR226468A1/es active
- 1981-07-02 PH PH25854A patent/PH17170A/en unknown
- 1981-07-02 IN IN425/DEL/81A patent/IN156779B/en unknown
- 1981-07-02 ES ES81503612A patent/ES8203929A1/es not_active Expired
- 1981-07-03 CA CA000381076A patent/CA1179436A/en not_active Expired
- 1981-07-03 BE BE0/205318A patent/BE889512A/fr not_active IP Right Cessation
- 1981-07-03 ZW ZW153/81A patent/ZW15381A1/xx unknown
- 1981-07-03 YU YU01650/81A patent/YU165081A/xx unknown
- 1981-07-03 KR KR1019810002430A patent/KR840001789B1/ko not_active Expired
- 1981-07-03 PL PL1981232028A patent/PL131741B1/pl unknown
- 1981-07-03 PT PT73317A patent/PT73317B/pt unknown
- 1981-07-03 CS CS815162A patent/CS243466B2/cs unknown
- 1981-07-03 IE IE1505/81A patent/IE51369B1/en unknown
- 1981-07-03 IT IT8122738A patent/IT1211074B/it active
- 1981-07-06 US US06/280,314 patent/US4373054A/en not_active Expired - Fee Related
- 1981-07-10 RO RO104833A patent/RO83379B/ro unknown
-
1984
- 1984-07-26 KR KR1019840004460A patent/KR840001790B1/ko not_active Expired
-
1987
- 1987-12-30 MY MY282/87A patent/MY8700282A/xx unknown
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