NO314945B1 - Varmherdbare pulverbelegningsmidler og anvendelse av disse - Google Patents

Varmherdbare pulverbelegningsmidler og anvendelse av disse Download PDF

Info

Publication number: NO314945B1
Authority: NO; Norway
Prior art keywords: acid; coating agents; agents according; weight; semi
Prior art date: 1995-12-06

Application number

NO19982551A

Other languages

English (en)

Norwegian (no)

Other versions

NO982551D0 (no

NO982551L (no

Inventor

Luc Moens

Daniel Maetens

Patrick Loosen

Jean-Marie Loutz

Original Assignee

Ucb Sa

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.)

1995-12-06

Filing date

1998-06-04

Publication date

2003-06-16

1998-06-04 Application filed by Ucb Sa filed Critical Ucb Sa

1998-06-04 Publication of NO982551D0 publication Critical patent/NO982551D0/no

1998-08-05 Publication of NO982551L publication Critical patent/NO982551L/no

2003-06-16 Publication of NO314945B1 publication Critical patent/NO314945B1/no

Links

239000000843 powder Substances 0.000 title claims abstract description 70
238000000576 coating method Methods 0.000 title claims abstract description 58
229920000728 polyester Polymers 0.000 claims abstract description 231
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 66
239000002253 acid Substances 0.000 claims abstract description 51
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims abstract description 48
239000000203 mixture Substances 0.000 claims abstract description 42
229920001187 thermosetting polymer Polymers 0.000 claims abstract description 37
239000003431 cross linking reagent Substances 0.000 claims abstract description 34
125000001931 aliphatic group Chemical group 0.000 claims abstract description 28
150000007513 acids Chemical class 0.000 claims abstract description 14
PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 claims abstract description 14
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims abstract description 13
229920005862 polyol Polymers 0.000 claims abstract description 13
150000003077 polyols Chemical class 0.000 claims abstract description 12
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims abstract description 11
239000011230 binding agent Substances 0.000 claims abstract description 10
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
125000003118 aryl group Chemical group 0.000 claims abstract description 9
DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 claims abstract description 7
150000001298 alcohols Chemical class 0.000 claims abstract description 7
125000000524 functional group Chemical group 0.000 claims abstract description 5
239000011248 coating agent Substances 0.000 claims description 66
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 26
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238000000034 method Methods 0.000 claims description 15
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BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 8
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CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 claims description 8
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OUPZKGBUJRBPGC-UHFFFAOYSA-N 1,3,5-tris(oxiran-2-ylmethyl)-1,3,5-triazinane-2,4,6-trione Chemical compound O=C1N(CC2OC2)C(=O)N(CC2OC2)C(=O)N1CC1CO1 OUPZKGBUJRBPGC-UHFFFAOYSA-N 0.000 claims description 7
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RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 4
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KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 4
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WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 4
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239000003381 stabilizer Substances 0.000 claims description 4
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 claims description 4
SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 claims description 3
229920006243 acrylic copolymer Polymers 0.000 claims description 3
150000001412 amines Chemical class 0.000 claims description 3
239000001530 fumaric acid Substances 0.000 claims description 3
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229910052751 metal Inorganic materials 0.000 claims description 3
239000002184 metal Substances 0.000 claims description 3
QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 claims description 2
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230000005855 radiation Effects 0.000 claims description 2
QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 claims 1
XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 claims 1
229920006395 saturated elastomer Polymers 0.000 claims 1
239000000463 material Substances 0.000 abstract description 60
239000003973 paint Substances 0.000 abstract description 19
238000004519 manufacturing process Methods 0.000 abstract description 17
239000002966 varnish Substances 0.000 abstract description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 description 16
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
230000015572 biosynthetic process Effects 0.000 description 12
238000003786 synthesis reaction Methods 0.000 description 11
FAOSYNUKPVJLNZ-UHFFFAOYSA-N butylstannane Chemical compound CCCC[SnH3] FAOSYNUKPVJLNZ-UHFFFAOYSA-N 0.000 description 10
238000006243 chemical reaction Methods 0.000 description 9
238000009998 heat setting Methods 0.000 description 9
239000011541 reaction mixture Substances 0.000 description 9
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238000003756 stirring Methods 0.000 description 8
238000000113 differential scanning calorimetry Methods 0.000 description 7
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238000005886 esterification reaction Methods 0.000 description 6
238000009472 formulation Methods 0.000 description 6
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150000002009 diols Chemical class 0.000 description 5
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238000010438 heat treatment Methods 0.000 description 5
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XTTGYFREQJCEML-UHFFFAOYSA-N tributyl phosphite Chemical compound CCCCOP(OCCCC)OCCCC XTTGYFREQJCEML-UHFFFAOYSA-N 0.000 description 5
FLPKSBDJMLUTEX-UHFFFAOYSA-N bis(1,2,2,6,6-pentamethylpiperidin-4-yl) 2-butyl-2-[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]propanedioate Chemical compound C1C(C)(C)N(C)C(C)(C)CC1OC(=O)C(C(=O)OC1CC(C)(C)N(C)C(C)(C)C1)(CCCC)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 FLPKSBDJMLUTEX-UHFFFAOYSA-N 0.000 description 4
239000000178 monomer Substances 0.000 description 4
239000000049 pigment Substances 0.000 description 4
238000012360 testing method Methods 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
239000004593 Epoxy Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
JHYNXXDQQHTCHJ-UHFFFAOYSA-M ethyl(triphenyl)phosphanium;bromide Chemical compound [Br-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(CC)C1=CC=CC=C1 JHYNXXDQQHTCHJ-UHFFFAOYSA-M 0.000 description 3
UJRDRFZCRQNLJM-UHFFFAOYSA-N methyl 3-[3-(benzotriazol-2-yl)-5-tert-butyl-4-hydroxyphenyl]propanoate Chemical compound CC(C)(C)C1=CC(CCC(=O)OC)=CC(N2N=C3C=CC=CC3=N2)=C1O UJRDRFZCRQNLJM-UHFFFAOYSA-N 0.000 description 3
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WTKWFNIIIXNTDO-UHFFFAOYSA-N 3-isocyanato-5-methyl-2-(trifluoromethyl)furan Chemical compound CC1=CC(N=C=O)=C(C(F)(F)F)O1 WTKWFNIIIXNTDO-UHFFFAOYSA-N 0.000 description 2
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238000000227 grinding Methods 0.000 description 1
235000019382 gum benzoic Nutrition 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
239000007788 liquid Substances 0.000 description 1
210000004185 liver Anatomy 0.000 description 1
238000005259 measurement Methods 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
239000012764 mineral filler Substances 0.000 description 1
OKRNLSUTBJUVKA-UHFFFAOYSA-N n,n,n',n'-Tetrakis(2-hydroxyethyl)adipamide Chemical compound OCCN(CCO)C(=O)CCCCC(=O)N(CCO)CCO OKRNLSUTBJUVKA-UHFFFAOYSA-N 0.000 description 1
ZBJVLWIYKOAYQH-UHFFFAOYSA-N naphthalen-2-yl 2-hydroxybenzoate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=C(C=CC=C2)C2=C1 ZBJVLWIYKOAYQH-UHFFFAOYSA-N 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
150000003003 phosphines Chemical class 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920000647 polyepoxide Polymers 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000011160 research Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
FBEVECUEMUUFKM-UHFFFAOYSA-M tetrapropylazanium;chloride Chemical compound [Cl-].CCC[N+](CCC)(CCC)CCC FBEVECUEMUUFKM-UHFFFAOYSA-M 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
150000004072 triols Chemical class 0.000 description 1
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000011787 zinc oxide Substances 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- 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
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Paints Or Removers (AREA)
Polyesters Or Polycarbonates (AREA)
Compositions Of Macromolecular Compounds (AREA)

NO19982551A 1995-12-06 1998-06-04 Varmherdbare pulverbelegningsmidler og anvendelse av disse NO314945B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
BE9501000A BE1009779A4 (fr)	1995-12-06	1995-12-06	Compositions thermodurcissables en poudre pour revetements.
PCT/BE1996/000127 WO1997020895A1 (fr)	1995-12-06	1996-12-05	Compositions thermodurcissables en poudre pour revetements

Publications (3)

Publication Number	Publication Date
NO982551D0 NO982551D0 (no)	1998-06-04
NO982551L NO982551L (no)	1998-08-05
NO314945B1 true NO314945B1 (no)	2003-06-16

Family

ID=3889332

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19982551A NO314945B1 (no)	1995-12-06	1998-06-04	Varmherdbare pulverbelegningsmidler og anvendelse av disse

Country Status (22)

Country	Link
US (1)	US6635721B1 (es)
EP (1)	EP0865470B1 (es)
JP (1)	JP2000501441A (es)
KR (1)	KR100432703B1 (es)
CN (1)	CN1077127C (es)
AR (1)	AR004982A1 (es)
AT (1)	ATE235539T1 (es)
AU (1)	AU710516B2 (es)
BE (1)	BE1009779A4 (es)
BR (1)	BR9611696A (es)
CA (1)	CA2238435A1 (es)
DE (1)	DE69627010T2 (es)
EA (1)	EA000690B1 (es)
ES (1)	ES2191122T3 (es)
IL (1)	IL124553A (es)
MY (1)	MY115645A (es)
NO (1)	NO314945B1 (es)
NZ (1)	NZ323341A (es)
PL (1)	PL184324B1 (es)
TR (1)	TR199800999T2 (es)
TW (1)	TW364922B (es)
WO (1)	WO1997020895A1 (es)

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BE1011628A3 (fr)	1997-12-18	1999-11-09	Ucb Sa	Compositions thermodurcissables en poudre pour la preparation de revetements de faible brillant.
EP1067159A1 (en) *	1999-07-02	2001-01-10	Ucb, S.A.	Thermosetting compositions for powder coatings
EP1358287A1 (en) *	2000-12-21	2003-11-05	Ucb, S.A.	Powdered thermosetting composition for coatings
EP1257606B1 (en) *	2000-12-21	2005-03-16	Surface Specialties, S.A.	Powdered thermosetting composition for coatings
JP2002265765A (ja) *	2001-03-08	2002-09-18	Toagosei Co Ltd	ポリエステル組成物
WO2002100956A1 (fr) *	2001-06-08	2002-12-19	Daikin Industries, Ltd.	Composition de revetement en poudre thermodurcissable
WO2003004574A1 (en) *	2001-07-02	2003-01-16	Ucb, S.A.	Thermosetting powder compositions for coatings
US20040087736A1 (en) *	2002-11-04	2004-05-06	Bin Wu	Powder coating compositions containing anhydride end-capped crystalline polyesters
US20040143073A1 (en) *	2003-01-15	2004-07-22	Imir Bejko	Method for determining gloss in polyester/beta-hydroxyalkylamide powder coatings
DE602004017846D1 (de) *	2003-03-20	2009-01-02	Cytec Surface Specialties Sa	Heisshärtbare pulverzusammensetzungen für lacke
ATE489440T1 (de) *	2003-03-20	2010-12-15	Cytec Surface Specialties Sa	Heisshärtbare pulverzusammensetzungen für beschichtungen
US7501150B2 (en) *	2004-01-28	2009-03-10	Xerox Corporation	Emulsion aggregation process for forming powder coating compositions, powder coating compositions and method for using the same
US7985524B2 (en) *	2004-01-28	2011-07-26	Xerox Corporation	Emulsion aggregation process for forming curable powder coating compositions, curable powder coating compositions and method for using the same
EP1571176A1 (en)	2004-03-01	2005-09-07	Mitsubishi Gas Chemical Company, Inc.	Resin composition with high vibration damping ability
US20060079650A1 (en) *	2004-10-12	2006-04-13	Stevenson Thomas A	Flexible, super durable powder coating composition
EP1726621A1 (en) *	2005-05-26	2006-11-29	Cytec Surface Specialties, S.A.	Thermosetting powder compositions
JP5326207B2 (ja) *	2006-12-15	2013-10-30	東洋紡株式会社	コーティング組成物、積層体及びフレキシブルフラットケーブル
EP2085441A1 (en) *	2008-01-31	2009-08-05	Cytec Surface Specialties, S.A.	Powder Composition
EP2085440A1 (en)	2008-01-31	2009-08-05	Cytec Italy, S.R.L.	Powder Compositions
EP2161294A1 (en)	2008-09-05	2010-03-10	Hexion Specialty Chemicals Research Belgium S.A.	Hydroxyl polyester resins with high Tg
EP2272927A1 (en) *	2009-07-07	2011-01-12	Cytec Surface Specialties, S.A.	Low temperature cure powder coating compositions
EP2330141A1 (en) *	2009-11-26	2011-06-08	Cytec Surface Specialties Austria GmbH	Polyester Resins
ES2500055T5 (es) *	2011-03-25	2018-02-13	Dsm Ip Assets B.V.	Composiciones de resina para composiciones de revestimiento en polvo termoendurecibles
MX369343B (es) *	2012-03-21	2019-11-06	Swimc Llc	Empaque de aplicacion para revestimiento en polvo.
JP2014122323A (ja) *	2012-10-31	2014-07-03	Dow Global Technologies Llc	金属包装のためのポリカーボネートコーティング
EP2740755A1 (en) *	2012-12-07	2014-06-11	Fonds de l'ESPCI - Georges Charpak	Processable semi-crystalline polymer networks
US10336925B2 (en) *	2015-09-08	2019-07-02	Resinate Materials Group, Inc.	Polyester polyols for reactive hot-melt adhesives
MX2018008550A (es) *	2016-01-15	2018-11-09	Ppg Ind Ohio Inc	Una composicion de revestimiento que comprende una resina termoendurecible y una resina termoplastica.
WO2017167450A1 (de)	2016-03-30	2017-10-05	Eckart Gmbh	Mit organischen bindemitteln für pulverlacke beschichtete effektpigmenten, sowie ein verfahren zur herstellung dieser beschichteten effektpigmente und ihre verwendung
CN106634479B (zh) *	2016-12-30	2019-05-14	山东麦都孚新材料科技有限公司	超临界流体技术制备的金属卷材用超耐候微球形粉末涂料及其制备方法
JP7069926B2 (ja) *	2018-03-26	2022-05-18	三菱ケミカル株式会社	ポリエステル樹脂組成物、インキ用バインダー及びインキ組成物
CN110591518B (zh) *	2019-09-27	2021-10-15	擎天材料科技有限公司	一种纯聚酯透明粉末涂料及其制备方法

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JPS59197426A (ja) *	1983-04-25	1984-11-09	Takeda Chem Ind Ltd	エポキシ基を有するポリエステル樹脂の製造法
US5182337A (en)	1986-09-29	1993-01-26	Ppg Industries, Inc.	Powder coating composition comprising a co-reactable particulate mixture of carboxylic acid group-containing polymers and beta-hydroxyalkylamide curing agent
US4889890A (en)	1987-12-30	1989-12-26	Ppg Industries, Inc.	Powder coating curing system containing a beta-hydroxyalkylamide
JP2819418B2 (ja) *	1988-10-18	1998-10-30	ダイセル化学工業株式会社	粉体塗料組成物のポットライフを改善する方法
GB9006737D0 (en) *	1990-03-26	1990-05-23	Courtaulds Coatings Ltd	Coating compositions
US5097006A (en)	1990-11-21	1992-03-17	U C B S.A.	Weatherable powder coating compositions
DE69222753T2 (de)	1992-03-16	1998-03-26	Ucb Sa	Cycloaliphatische Polyester mit Carboxylendgruppen zur Darstellung von Pulverlacken
WO1994002552A1 (en)	1992-07-21	1994-02-03	Eastman Chemical Company	Thermosetting powder coating compositions
US5728779A (en)	1992-12-01	1998-03-17	Dsm N.V.	Powder paint of epoxy-reactive polymer and aliphatic chain-containing polyepoxide
EP0706545B1 (en)	1993-07-01	1997-03-05	Eastman Chemical Company	Thermosetting coating compositions
KR960703420A (ko)	1993-07-01	1996-08-17	해리 제이. 그윈넬	분말 피복 조성물(powder coating compositions)

1995
- 1995-12-06 BE BE9501000A patent/BE1009779A4/fr not_active IP Right Cessation
1996
- 1996-11-19 MY MYPI96004818A patent/MY115645A/en unknown
- 1996-11-29 AR ARP960105413A patent/AR004982A1/es active IP Right Grant
- 1996-12-05 BR BR9611696-0A patent/BR9611696A/pt not_active IP Right Cessation
- 1996-12-05 AT AT96940944T patent/ATE235539T1/de not_active IP Right Cessation
- 1996-12-05 JP JP9520804A patent/JP2000501441A/ja not_active Ceased
- 1996-12-05 AU AU10262/97A patent/AU710516B2/en not_active Ceased
- 1996-12-05 NZ NZ323341A patent/NZ323341A/en unknown
- 1996-12-05 CA CA002238435A patent/CA2238435A1/fr not_active Abandoned
- 1996-12-05 EA EA199800509A patent/EA000690B1/ru not_active IP Right Cessation
- 1996-12-05 TR TR1998/00999T patent/TR199800999T2/xx unknown
- 1996-12-05 CN CN96198843A patent/CN1077127C/zh not_active Expired - Fee Related
- 1996-12-05 EP EP96940944A patent/EP0865470B1/fr not_active Expired - Lifetime
- 1996-12-05 ES ES96940944T patent/ES2191122T3/es not_active Expired - Lifetime
- 1996-12-05 PL PL96327180A patent/PL184324B1/pl not_active IP Right Cessation
- 1996-12-05 IL IL12455396A patent/IL124553A/xx not_active IP Right Cessation
- 1996-12-05 WO PCT/BE1996/000127 patent/WO1997020895A1/fr active IP Right Grant
- 1996-12-05 DE DE69627010T patent/DE69627010T2/de not_active Expired - Fee Related
- 1996-12-05 KR KR10-1998-0704164A patent/KR100432703B1/ko not_active IP Right Cessation
- 1996-12-06 TW TW085115079A patent/TW364922B/zh active
1998
- 1998-06-04 NO NO19982551A patent/NO314945B1/no unknown
2000
- 2000-09-18 US US09/664,451 patent/US6635721B1/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
IL124553A0 (en)	1998-12-06
AU710516B2 (en)	1999-09-23
EA000690B1 (ru)	2000-02-28
DE69627010T2 (de)	2003-12-11
EA199800509A1 (ru)	1998-12-24
BR9611696A (pt)	1999-12-28
KR100432703B1 (ko)	2005-05-19
CA2238435A1 (fr)	1997-06-12
PL327180A1 (en)	1998-11-23
PL184324B1 (pl)	2002-10-31
EP0865470A1 (fr)	1998-09-23
KR19990071879A (ko)	1999-09-27
JP2000501441A (ja)	2000-02-08
DE69627010D1 (de)	2003-04-30
NO982551D0 (no)	1998-06-04
AU1026297A (en)	1997-06-27
CN1203619A (zh)	1998-12-30
WO1997020895A1 (fr)	1997-06-12
NO982551L (no)	1998-08-05
MY115645A (en)	2003-08-30
NZ323341A (en)	1999-09-29
ES2191122T3 (es)	2003-09-01
IL124553A (en)	2001-08-26
CN1077127C (zh)	2002-01-02
EP0865470B1 (fr)	2003-03-26
TR199800999T2 (xx)	1998-09-21
AR004982A1 (es)	1999-04-07
ATE235539T1 (de)	2003-04-15
BE1009779A4 (fr)	1997-08-05
TW364922B (en)	1999-07-21
US6635721B1 (en)	2003-10-21

Publication	Publication Date	Title
NO314945B1 (no)	2003-06-16	Varmherdbare pulverbelegningsmidler og anvendelse av disse
US7951427B2 (en)	2011-05-31	Thermosetting powder compositions
US6844072B2 (en)	2005-01-18	Powdered thermosetting composition for coatings
US5525370A (en)	1996-06-11	Process for the preparation of matte coatings using powdered thermosetting compositions
US20030166793A1 (en)	2003-09-04	Powdered thermosetting composition for coatings
MXPA04012498A (es)	2005-07-14	Composiciones de recubrimiento en polvo semi-brillante.
TW568924B (en)	2004-01-01	Polyester containing tertiary carboxyl groups, process for its preparation and thermosetting powder compositions containing it
US20060217520A1 (en)	2006-09-28	Thermosetting powder compositions for coatings
WO2009106454A1 (en)	2009-09-03	Powder compositions
WO2002085999A1 (en)	2002-10-31	Thermosetting powder compositions for coatings
WO2003004574A1 (en)	2003-01-16	Thermosetting powder compositions for coatings
WO2004026981A1 (en)	2004-04-01	BINDER COMPOSITION COMPRISING A CARBOXYL FUNCTIONAL POLYESTER AND A β-HYDROXY ALKYL AMIDE