SK33998A3 - Precross-linked silicone elastomer particles with organopolymer shell as formulation constituent in powder coating materials - Google Patents

Precross-linked silicone elastomer particles with organopolymer shell as formulation constituent in powder coating materials Download PDF

Info

Publication number: SK33998A3
Authority: SK; Slovakia
Prior art keywords: silicone elastomer; elastomer particles; weight; organic polymer; mol
Prior art date: 1995-09-26

Application number

SK339-98A

Other languages

English (en)

Slovak (sk)

Inventor

Michael Geck

Walter Goeblmeier

Bernward Deubzer

Ekkehard Patrick

Original Assignee

Wacker Chemie Gmbh

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.)

1995-09-26

Filing date

1996-09-26

Publication date

1998-08-05

1996-09-26 Application filed by Wacker Chemie Gmbh filed Critical Wacker Chemie Gmbh

1998-08-05 Publication of SK33998A3 publication Critical patent/SK33998A3/sk

Links

239000000843 powder Substances 0.000 title claims abstract description 49
239000002245 particle Substances 0.000 title claims abstract description 47
238000000576 coating method Methods 0.000 title claims abstract description 44
229920002379 silicone rubber Polymers 0.000 title claims abstract description 34
239000011248 coating agent Substances 0.000 title claims abstract description 31
239000000203 mixture Substances 0.000 title claims abstract description 18
239000000463 material Substances 0.000 title abstract description 7
239000000470 constituent Substances 0.000 title abstract 2
238000009472 formulation Methods 0.000 title abstract 2
229920000642 polymer Polymers 0.000 claims abstract description 26
239000011230 binding agent Substances 0.000 claims abstract description 25
229920001187 thermosetting polymer Polymers 0.000 claims abstract description 16
229920001169 thermoplastic Polymers 0.000 claims abstract description 15
239000004416 thermosoftening plastic Substances 0.000 claims abstract description 15
229920001577 copolymer Polymers 0.000 claims abstract description 13
239000000178 monomer Substances 0.000 claims abstract description 11
-1 alkenyl radicals Chemical class 0.000 claims description 35
229920000620 organic polymer Polymers 0.000 claims description 30
239000008199 coating composition Substances 0.000 claims description 15
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
229920003229 poly(methyl methacrylate) Chemical group 0.000 claims description 8
239000004926 polymethyl methacrylate Chemical group 0.000 claims description 8
229910004283 SiO 4 Inorganic materials 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 6
239000004215 Carbon black (E152) Substances 0.000 claims description 5
229910004298 SiO 2 Inorganic materials 0.000 claims description 5
150000005840 aryl radicals Chemical class 0.000 claims description 5
229930195733 hydrocarbon Natural products 0.000 claims description 5
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 4
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 3
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 claims description 3
238000009826 distribution Methods 0.000 claims description 3
125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
229910020485 SiO4/2 Inorganic materials 0.000 abstract 1
125000003342 alkenyl group Chemical group 0.000 abstract 1
125000001183 hydrocarbyl group Chemical group 0.000 abstract 1
229920001296 polysiloxane Polymers 0.000 description 14
238000000034 method Methods 0.000 description 10
239000011347 resin Substances 0.000 description 8
229920005989 resin Polymers 0.000 description 7
238000012360 testing method Methods 0.000 description 7
239000000654 additive Substances 0.000 description 6
239000003607 modifier Substances 0.000 description 6
230000008569 process Effects 0.000 description 6
BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 5
238000004132 cross linking Methods 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
229920001225 polyester resin Polymers 0.000 description 5
239000004645 polyester resin Substances 0.000 description 5
229910000077 silane Inorganic materials 0.000 description 5
239000004593 Epoxy Substances 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
239000004922 lacquer Substances 0.000 description 4
238000012545 processing Methods 0.000 description 4
150000004756 silanes Chemical class 0.000 description 4
229920002050 silicone resin Polymers 0.000 description 4
238000005245 sintering Methods 0.000 description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
239000004698 Polyethylene Substances 0.000 description 3
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
239000000853 adhesive Substances 0.000 description 3
230000001070 adhesive effect Effects 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000011109 contamination Methods 0.000 description 3
238000007720 emulsion polymerization reaction Methods 0.000 description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
239000011159 matrix material Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
238000002156 mixing Methods 0.000 description 3
239000000049 pigment Substances 0.000 description 3
229920000647 polyepoxide Polymers 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
238000000926 separation method Methods 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
238000010304 firing Methods 0.000 description 2
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 2
238000004519 manufacturing process Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
239000004848 polyfunctional curative Substances 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
229920005749 polyurethane resin Polymers 0.000 description 2
BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
230000009467 reduction Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
125000006039 1-hexenyl group Chemical group 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
UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
239000004925 Acrylic resin Substances 0.000 description 1
229920000178 Acrylic resin Polymers 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
229920003319 Araldite® Polymers 0.000 description 1
OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
108010020147 Protein Corona Proteins 0.000 description 1
BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
125000005396 acrylic acid ester group Chemical group 0.000 description 1
239000002390 adhesive tape Substances 0.000 description 1
230000002411 adverse Effects 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
230000005587 bubbling Effects 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
238000003490 calendering Methods 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
238000009750 centrifugal casting Methods 0.000 description 1
YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000013329 compounding Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000010276 construction Methods 0.000 description 1
230000007547 defect Effects 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
JJQZDUKDJDQPMQ-UHFFFAOYSA-N dimethoxy(dimethyl)silane Chemical compound CO[Si](C)(C)OC JJQZDUKDJDQPMQ-UHFFFAOYSA-N 0.000 description 1
YYLGKUPAFFKGRQ-UHFFFAOYSA-N dimethyldiethoxysilane Chemical compound CCO[Si](C)(C)OCC YYLGKUPAFFKGRQ-UHFFFAOYSA-N 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
229920001971 elastomer Polymers 0.000 description 1
238000009503 electrostatic coating Methods 0.000 description 1
238000004924 electrostatic deposition Methods 0.000 description 1
238000007590 electrostatic spraying Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
125000003700 epoxy group Chemical group 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
239000000945 filler Substances 0.000 description 1
GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
238000000227 grinding Methods 0.000 description 1
HTDJPCNNEPUOOQ-UHFFFAOYSA-N hexamethylcyclotrisiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O1 HTDJPCNNEPUOOQ-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000009863 impact test Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000003999 initiator Substances 0.000 description 1
238000011081 inoculation Methods 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
238000002955 isolation Methods 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000004898 kneading Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
BFXIKLCIZHOAAZ-UHFFFAOYSA-N methyltrimethoxysilane Chemical compound CO[Si](C)(OC)OC BFXIKLCIZHOAAZ-UHFFFAOYSA-N 0.000 description 1
239000011859 microparticle Substances 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000005012 migration Effects 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000010899 nucleation Methods 0.000 description 1
HMMGMWAXVFQUOA-UHFFFAOYSA-N octamethylcyclotetrasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 HMMGMWAXVFQUOA-UHFFFAOYSA-N 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
238000005191 phase separation Methods 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920013716 polyethylene resin Polymers 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000011164 primary particle Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
239000005060 rubber Substances 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229920005573 silicon-containing polymer Polymers 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
238000010998 test method Methods 0.000 description 1
LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
JCVQKRGIASEUKR-UHFFFAOYSA-N triethoxy(phenyl)silane Chemical compound CCO[Si](OCC)(OCC)C1=CC=CC=C1 JCVQKRGIASEUKR-UHFFFAOYSA-N 0.000 description 1
238000002255 vaccination Methods 0.000 description 1
229960000834 vinyl ether Drugs 0.000 description 1

Classifications

- 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
- C09D151/00—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers
- C09D151/08—Coating compositions based on graft polymers in which the grafted component is obtained by reactions only involving carbon-to-carbon unsaturated bonds; Coating compositions based on derivatives of such polymers grafted on to macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- 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
- C08F283/12—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polysiloxanes
- 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
- C09D5/03—Powdery paints
- 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
- C09D5/03—Powdery paints
- C09D5/033—Powdery paints characterised by the additives
- C09D5/037—Rheology improving agents, e.g. flow control agents
- 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
- Y10S525/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S525/902—Core-shell

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
Wood Science & Technology (AREA)
Materials Engineering (AREA)
Life Sciences & Earth Sciences (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Paints Or Removers (AREA)
Silicon Polymers (AREA)
Compositions Of Macromolecular Compounds (AREA)
Graft Or Block Polymers (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Adhesives Or Adhesive Processes (AREA)

SK339-98A 1995-09-26 1996-09-26 Precross-linked silicone elastomer particles with organopolymer shell as formulation constituent in powder coating materials SK33998A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19535824A DE19535824A1 (de)	1995-09-26	1995-09-26	Vorvernetzte Siliconelastomer-Partikel mit Organopolymerhülle als Formulierungsbestandteil in Pulverlacken
PCT/EP1996/004208 WO1997012005A1 (de)	1995-09-26	1996-09-26	Vorvernetzte siliconelastomer-partikel mit organopolymerhülle als formulierungsbestandteil in pulverlacken

Publications (1)

Publication Number	Publication Date
SK33998A3 true SK33998A3 (en)	1998-08-05

Family

ID=7773249

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK339-98A SK33998A3 (en)	1995-09-26	1996-09-26	Precross-linked silicone elastomer particles with organopolymer shell as formulation constituent in powder coating materials

Country Status (20)

Country	Link
US (1)	US5981659A (cs)
EP (1)	EP0852610B1 (cs)
JP (1)	JP3299972B2 (cs)
KR (1)	KR100275285B1 (cs)
CN (1)	CN1070902C (cs)
AT (1)	ATE180506T1 (cs)
AU (1)	AU705522B2 (cs)
BR (1)	BR9610711A (cs)
CA (1)	CA2232067A1 (cs)
CZ (1)	CZ288425B6 (cs)
DE (2)	DE19535824A1 (cs)
DK (1)	DK0852610T3 (cs)
ES (1)	ES2134008T3 (cs)
NO (1)	NO981330D0 (cs)
PL (1)	PL184033B1 (cs)
RU (1)	RU2152969C1 (cs)
SK (1)	SK33998A3 (cs)
TW (1)	TW399089B (cs)
WO (1)	WO1997012005A1 (cs)
ZA (1)	ZA967978B (cs)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE19617379A1 (de) *	1996-04-30	1997-11-06	Wacker Chemie Gmbh	Vorvernetzte Siliconelastomer-Partikel mit Organopolymerhülle als Formulierungsbestandteil in wäßrigen Lackzubereitungen
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1995
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1996
- 1996-08-21 TW TW085110224A patent/TW399089B/zh not_active IP Right Cessation
- 1996-09-20 ZA ZA967978A patent/ZA967978B/xx unknown
- 1996-09-26 DE DE59602023T patent/DE59602023D1/de not_active Expired - Fee Related
- 1996-09-26 DK DK96933401T patent/DK0852610T3/da active
- 1996-09-26 PL PL96325969A patent/PL184033B1/pl unknown
- 1996-09-26 RU RU98107839/04A patent/RU2152969C1/ru active
- 1996-09-26 EP EP96933401A patent/EP0852610B1/de not_active Expired - Lifetime
- 1996-09-26 AU AU72150/96A patent/AU705522B2/en not_active Ceased
- 1996-09-26 ES ES96933401T patent/ES2134008T3/es not_active Expired - Lifetime
- 1996-09-26 KR KR1019980701919A patent/KR100275285B1/ko not_active Expired - Fee Related
- 1996-09-26 SK SK339-98A patent/SK33998A3/sk unknown
- 1996-09-26 CN CN96196234A patent/CN1070902C/zh not_active Expired - Fee Related
- 1996-09-26 CZ CZ1998925A patent/CZ288425B6/cs not_active IP Right Cessation
- 1996-09-26 JP JP51314597A patent/JP3299972B2/ja not_active Expired - Fee Related
- 1996-09-26 US US09/029,552 patent/US5981659A/en not_active Expired - Fee Related
- 1996-09-26 CA CA002232067A patent/CA2232067A1/en not_active Abandoned
- 1996-09-26 WO PCT/EP1996/004208 patent/WO1997012005A1/de not_active Ceased
- 1996-09-26 AT AT96933401T patent/ATE180506T1/de not_active IP Right Cessation
- 1996-09-26 BR BR9610711A patent/BR9610711A/pt active Search and Examination
1998
- 1998-03-24 NO NO981330A patent/NO981330D0/no not_active Application Discontinuation

Also Published As

Publication number	Publication date
PL184033B1 (pl)	2002-08-30
AU7215096A (en)	1997-04-17
JP3299972B2 (ja)	2002-07-08
CA2232067A1 (en)	1997-04-03
ES2134008T3 (es)	1999-09-16
JPH11500175A (ja)	1999-01-06
WO1997012005A1 (de)	1997-04-03
ZA967978B (en)	1997-03-26
DK0852610T3 (da)	1999-11-08
CZ288425B6 (en)	2001-06-13
NO981330L (no)	1998-03-24
KR19990044665A (ko)	1999-06-25
ATE180506T1 (de)	1999-06-15
BR9610711A (pt)	1999-07-13
TW399089B (en)	2000-07-21
CZ92598A3 (cs)	1998-06-17
AU705522B2 (en)	1999-05-27
NO981330D0 (no)	1998-03-24
EP0852610A1 (de)	1998-07-15
RU2152969C1 (ru)	2000-07-20
EP0852610B1 (de)	1999-05-26
CN1070902C (zh)	2001-09-12
DE59602023D1 (de)	1999-07-01
CN1192767A (zh)	1998-09-09
US5981659A (en)	1999-11-09
KR100275285B1 (ko)	2000-12-15
DE19535824A1 (de)	1997-03-27
PL325969A1 (en)	1998-08-17

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