NL1011403C2 - Bindmiddelsamenstelling voor poederverven. - Google Patents

Bindmiddelsamenstelling voor poederverven. Download PDF

Info

Publication number: NL1011403C2
Authority: NL; Netherlands
Prior art keywords: acid; catalyst; alkyl; aryl; composition according
Prior art date: 1999-02-26

Application number

NL1011403A

Other languages

English (en)

Dutch (nl)

Inventor

Johan Rietberg

Rudolfus Antonius Theo Benthem

Patrick Herman Marie Hendriks

Original Assignee

Dsm Nv

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.)

1999-02-26

Filing date

1999-02-26

Publication date

2000-08-29

1999-02-26 Application filed by Dsm Nv filed Critical Dsm Nv

1999-02-26 Priority to NL1011403A priority Critical patent/NL1011403C2/nl

2000-02-24 Priority to CN00806685A priority patent/CN1348484A/zh

2000-02-24 Priority to EP00908103A priority patent/EP1165703A1/fr

2000-02-24 Priority to PCT/NL2000/000120 priority patent/WO2000050520A1/fr

2000-02-24 Priority to AU29475/00A priority patent/AU2947500A/en

2000-02-24 Priority to JP2000601088A priority patent/JP2002537469A/ja

2000-08-29 Application granted granted Critical

2000-08-29 Publication of NL1011403C2 publication Critical patent/NL1011403C2/nl

2001-08-23 Priority to US09/934,682 priority patent/US20020019467A1/en

Links

239000000843 powder Substances 0.000 title claims description 24
239000000203 mixture Substances 0.000 title claims description 22
239000003973 paint Substances 0.000 title claims description 17
239000011230 binding agent Substances 0.000 title claims description 10
150000001875 compounds Chemical class 0.000 claims description 24
239000003054 catalyst Substances 0.000 claims description 17
238000000576 coating method Methods 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 13
ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 8
239000011248 coating agent Substances 0.000 claims description 7
125000006736 (C6-C20) aryl group Chemical group 0.000 claims description 6
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 4
150000001735 carboxylic acids Chemical group 0.000 claims description 4
150000008064 anhydrides Chemical class 0.000 claims description 3
150000002148 esters Chemical class 0.000 claims description 3
MLCHBQKMVKNBOV-UHFFFAOYSA-N phenylphosphinic acid Chemical compound OP(=O)C1=CC=CC=C1 MLCHBQKMVKNBOV-UHFFFAOYSA-N 0.000 claims description 3
239000000758 substrate Substances 0.000 claims description 3
150000007513 acids Chemical class 0.000 claims description 2
238000000034 method Methods 0.000 claims 2
125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 1
238000011835 investigation Methods 0.000 claims 1
230000000153 supplemental effect Effects 0.000 claims 1
-1 for example Chemical compound 0.000 description 22
229920000642 polymer Polymers 0.000 description 15
125000004432 carbon atom Chemical group C* 0.000 description 9
125000003118 aryl group Chemical group 0.000 description 8
239000001257 hydrogen Substances 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
229920000728 polyester Polymers 0.000 description 5
125000000041 C6-C10 aryl group Chemical group 0.000 description 4
239000000654 additive Substances 0.000 description 4
ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
239000000049 pigment Substances 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
239000004971 Cross linker Substances 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
229920001187 thermosetting polymer Polymers 0.000 description 3
125000003837 (C1-C20) alkyl group Chemical group 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-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
229910003953 H3PO2 Inorganic materials 0.000 description 2
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical group ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 2
UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
244000028419 Styrax benzoin Species 0.000 description 2
235000000126 Styrax benzoin Nutrition 0.000 description 2
235000008411 Sumatra benzointree Nutrition 0.000 description 2
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
229960002130 benzoin Drugs 0.000 description 2
125000002843 carboxylic acid group Chemical group 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
238000007872 degassing Methods 0.000 description 2
238000004821 distillation Methods 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
239000000945 filler Substances 0.000 description 2
235000019382 gum benzoic Nutrition 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
125000002768 hydroxyalkyl group Chemical group 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000000178 monomer Substances 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
125000000008 (C1-C10) alkyl group Chemical group 0.000 description 1
125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 description 1
125000006018 1-methyl-ethenyl group Chemical group 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
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 description 1
SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 description 1
229910014033 C-OH Inorganic materials 0.000 description 1
229910014570 C—OH Inorganic materials 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 1
239000005083 Zinc sulfide Substances 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
229920003232 aliphatic polyester Polymers 0.000 description 1
125000005080 alkoxycarbonylalkenyl group Chemical group 0.000 description 1
125000005599 alkyl carboxylate group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000001204 arachidyl 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])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])[H] 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
HBPTUDIZKSGJNN-UHFFFAOYSA-N benzoic acid;cyclohexane;methanol Chemical compound OC.OC.C1CCCCC1.OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1 HBPTUDIZKSGJNN-UHFFFAOYSA-N 0.000 description 1
JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000005019 carboxyalkenyl group Chemical group 0.000 description 1
229910000423 chromium oxide Inorganic materials 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 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
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000002704 decyl 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])* 0.000 description 1
LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
229940043276 diisopropanolamine Drugs 0.000 description 1
238000007590 electrostatic spraying Methods 0.000 description 1
230000004907 flux Effects 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
239000006115 industrial coating Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
238000011068 loading method Methods 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
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 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
238000002156 mixing Methods 0.000 description 1
125000001802 myricyl 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])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])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])[H] 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
UUCAVBDCVCFNIN-UHFFFAOYSA-N n,n,n',n'-tetrakis(2-hydroxypropyl)hexanediamide Chemical compound CC(O)CN(CC(C)O)C(=O)CCCCC(=O)N(CC(C)O)CC(C)O UUCAVBDCVCFNIN-UHFFFAOYSA-N 0.000 description 1
125000004108 n-butyl group Chemical group [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
125000001624 naphthyl group Chemical group 0.000 description 1
229910052757 nitrogen Inorganic materials 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
125000002347 octyl 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])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
150000002989 phenols 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
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
238000007639 printing Methods 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000004053 quinones Chemical class 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
238000003756 stirring Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
125000004417 unsaturated alkyl group Chemical group 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
239000002023 wood Substances 0.000 description 1
229910052984 zinc sulfide Inorganic materials 0.000 description 1
DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 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
- C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Organic Chemistry (AREA)
Paints Or Removers (AREA)

NL1011403A 1999-02-26 1999-02-26 Bindmiddelsamenstelling voor poederverven. NL1011403C2 (nl)

Priority Applications (7)

Application Number	Priority Date	Filing Date	Title
NL1011403A NL1011403C2 (nl)	1999-02-26	1999-02-26	Bindmiddelsamenstelling voor poederverven.
CN00806685A CN1348484A (zh)	1999-02-26	2000-02-24	用于粉末涂料的粘合剂组合物
EP00908103A EP1165703A1 (fr)	1999-02-26	2000-02-24	Composition liante pour revetements pulverulents
PCT/NL2000/000120 WO2000050520A1 (fr)	1999-02-26	2000-02-24	Composition liante pour revetements pulverulents
AU29475/00A AU2947500A (en)	1999-02-26	2000-02-24	Binder composition for powder coatings
JP2000601088A JP2002537469A (ja)	1999-02-26	2000-02-24	粉末コーティング用のバインダー組成物
US09/934,682 US20020019467A1 (en)	1999-02-26	2001-08-23	Binder composition for powder coatings

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL1011403		1999-02-26
NL1011403A NL1011403C2 (nl)	1999-02-26	1999-02-26	Bindmiddelsamenstelling voor poederverven.

Publications (1)

Publication Number	Publication Date
NL1011403C2 true NL1011403C2 (nl)	2000-08-29

Family

ID=19768731

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL1011403A NL1011403C2 (nl)	1999-02-26	1999-02-26	Bindmiddelsamenstelling voor poederverven.

Country Status (7)

Country	Link
US (1)	US20020019467A1 (fr)
EP (1)	EP1165703A1 (fr)
JP (1)	JP2002537469A (fr)
CN (1)	CN1348484A (fr)
AU (1)	AU2947500A (fr)
NL (1)	NL1011403C2 (fr)
WO (1)	WO2000050520A1 (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP1134266A1 (fr) *	2000-03-13	2001-09-19	Dsm N.V.	Composition de peinture en poudre
JP5244789B2 (ja) *	2006-05-02	2013-07-24	イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー	インクジェットインク、インクセットおよび印刷方法

Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1998030627A1 (fr) *	1997-01-07	1998-07-16	National Starch And Chemical Investment Holding Corporation	Agents de reticulation a base d'(hydroxyalkyl)uree

1999
- 1999-02-26 NL NL1011403A patent/NL1011403C2/nl not_active IP Right Cessation
2000
- 2000-02-24 EP EP00908103A patent/EP1165703A1/fr not_active Withdrawn
- 2000-02-24 CN CN00806685A patent/CN1348484A/zh active Pending
- 2000-02-24 JP JP2000601088A patent/JP2002537469A/ja active Pending
- 2000-02-24 WO PCT/NL2000/000120 patent/WO2000050520A1/fr not_active Ceased
- 2000-02-24 AU AU29475/00A patent/AU2947500A/en not_active Abandoned
2001
- 2001-08-23 US US09/934,682 patent/US20020019467A1/en not_active Abandoned

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1998030627A1 (fr) *	1997-01-07	1998-07-16	National Starch And Chemical Investment Holding Corporation	Agents de reticulation a base d'(hydroxyalkyl)uree

Also Published As

Publication number	Publication date
WO2000050520A1 (fr)	2000-08-31
EP1165703A1 (fr)	2002-01-02
AU2947500A (en)	2000-09-14
CN1348484A (zh)	2002-05-08
US20020019467A1 (en)	2002-02-14
JP2002537469A (ja)	2002-11-05

Publication	Publication Date	Title
NL1005809C2 (nl)	1998-10-19	Poederverfbindmiddelsamenstelling.
NL1007052C2 (nl)	1999-03-18	Bindmiddelsamenstelling voor poederverfformuleringen.
TW385328B (en)	2000-03-21	Corrosion inhibitors in powder coatings
JPH0573787B2 (fr)	1993-10-15
KR100989195B1 (ko)	2010-10-20	에스터 아마이드 축합 생성물을 포함하는 분말 코팅 소광제
DE602004005308T2 (de)	2007-12-20	Rtv-beschichtungszusammensetzung
CN101223250B (zh)	2012-08-29	粉末涂料组合物
NL1002153C2 (nl)	1997-08-04	Stralingsuithardbare poederverfbindmiddelsamenstelling.
PL173087B1 (pl)	1998-01-30	Termoutwardzalna proszkowa kompozycja powłokowa
CN100572473C (zh)	2009-12-23	辐射固化性低光泽粉末涂料组合物
AU664482B2 (en)	1995-11-16	Powder coating composition with hydroxyalkylamide crosslinker
JP4033453B2 (ja)	2008-01-16	粉体塗料組成物
NL1011403C2 (nl)	2000-08-29	Bindmiddelsamenstelling voor poederverven.
TW379245B (en)	2000-01-11	Curable coating compositions and process for coating a substrate
US20030186091A1 (en)	2003-10-02	Power paint composition
CN1636043A (zh)	2005-07-06	聚合物组合物
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