CA2209320C - Procede pour la production d'un revetement pulverulent - Google Patents

Procede pour la production d'un revetement pulverulent Download PDF

Info

Publication number: CA2209320C
Authority: CA; Canada
Prior art keywords: acid; meth; powder coating; acrylate; approximately
Prior art date: 1997-06-30
Legal status (The legal status 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 status listed.): Expired - Fee Related

Application number

CA002209320A

Other languages

English (en)

Other versions

CA2209320A1 (fr

Inventor

Takato Adachi

Nobushige Numa

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Kansai Paint Co Ltd

Original Assignee

Kansai Paint Co Ltd

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.)

1997-06-30

Filing date

1997-06-30

Publication date

2006-07-18

1997-06-30 Application filed by Kansai Paint Co Ltd filed Critical Kansai Paint Co Ltd

1997-06-30 Priority to CA002209320A priority Critical patent/CA2209320C/fr

1997-07-02 Priority to GB9714011A priority patent/GB2326883B/en

1998-12-30 Publication of CA2209320A1 publication Critical patent/CA2209320A1/fr

2006-07-18 Application granted granted Critical

2006-07-18 Publication of CA2209320C publication Critical patent/CA2209320C/fr

2017-06-30 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

238000000576 coating method Methods 0.000 title claims abstract description 71
239000011248 coating agent Substances 0.000 title claims abstract description 65
239000000843 powder Substances 0.000 title claims abstract description 46
238000000034 method Methods 0.000 title claims abstract description 34
238000004519 manufacturing process Methods 0.000 title claims abstract description 32
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 64
239000000178 monomer Substances 0.000 claims abstract description 61
DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims abstract description 40
239000002904 solvent Substances 0.000 claims abstract description 38
239000003431 cross linking reagent Substances 0.000 claims abstract description 27
239000000203 mixture Substances 0.000 claims abstract description 26
229920006163 vinyl copolymer Polymers 0.000 claims abstract description 16
125000000524 functional group Chemical group 0.000 claims abstract description 15
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
230000009477 glass transition Effects 0.000 claims abstract description 12
238000002844 melting Methods 0.000 claims abstract description 12
230000008018 melting Effects 0.000 claims abstract description 12
229920001187 thermosetting polymer Polymers 0.000 claims abstract description 8
229920001577 copolymer Polymers 0.000 claims abstract description 4
239000011347 resin Substances 0.000 claims description 22
229920005989 resin Polymers 0.000 claims description 22
239000002253 acid Substances 0.000 claims description 21
150000007513 acids Chemical class 0.000 claims description 14
-1 3,4-epoxycyclohexylmethyl Chemical group 0.000 claims description 12
238000004108 freeze drying Methods 0.000 claims description 10
239000000654 additive Substances 0.000 claims description 9
125000001931 aliphatic group Chemical group 0.000 claims description 9
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 8
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 8
150000008065 acid anhydrides Chemical class 0.000 claims description 8
239000003795 chemical substances by application Substances 0.000 claims description 7
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
125000002723 alicyclic group Chemical group 0.000 claims description 5
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 claims description 5
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 4
239000004593 Epoxy Substances 0.000 claims description 4
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 4
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
239000001530 fumaric acid Substances 0.000 claims description 4
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 claims description 4
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 4
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 claims description 4
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 claims description 4
ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 claims description 4
150000008064 anhydrides Chemical class 0.000 claims description 3
239000002981 blocking agent Substances 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
125000005397 methacrylic acid ester group Chemical group 0.000 claims description 3
238000002156 mixing Methods 0.000 claims description 3
DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical group C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 claims description 2
RHBGITBPARBDPH-UHFFFAOYSA-N (2E,4E)-5-(3,4-methylenedioxyphenyl)-2,4-pentadienoic acid Natural products OC(=O)C=CC=CC1=CC=C2OCOC2=C1 RHBGITBPARBDPH-UHFFFAOYSA-N 0.000 claims description 2
RHBGITBPARBDPH-ZPUQHVIOSA-N (E,E)-piperic acid Chemical compound OC(=O)\C=C\C=C\C1=CC=C2OCOC2=C1 RHBGITBPARBDPH-ZPUQHVIOSA-N 0.000 claims description 2
PMUPSYZVABJEKC-UHFFFAOYSA-N 1-methylcyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1(C)CCCCC1C(O)=O PMUPSYZVABJEKC-UHFFFAOYSA-N 0.000 claims description 2
RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 claims description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
LSWYGACWGAICNM-UHFFFAOYSA-N 2-(prop-2-enoxymethyl)oxirane Chemical compound C=CCOCC1CO1 LSWYGACWGAICNM-UHFFFAOYSA-N 0.000 claims description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
VUIWJRYTWUGOOF-UHFFFAOYSA-N 2-ethenoxyethanol Chemical class OCCOC=C VUIWJRYTWUGOOF-UHFFFAOYSA-N 0.000 claims description 2
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 2
239000006096 absorbing agent Substances 0.000 claims description 2
239000001361 adipic acid Substances 0.000 claims description 2
235000011037 adipic acid Nutrition 0.000 claims description 2
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
239000002518 antifoaming agent Substances 0.000 claims description 2
239000003963 antioxidant agent Substances 0.000 claims description 2
KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 claims description 2
HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims description 2
229940018557 citraconic acid Drugs 0.000 claims description 2
238000004040 coloring Methods 0.000 claims description 2
150000001875 compounds Chemical class 0.000 claims description 2
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 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 description 2
XBZSBBLNHFMTEB-UHFFFAOYSA-N cyclohexane-1,3-dicarboxylic acid Chemical compound OC(=O)C1CCCC(C(O)=O)C1 XBZSBBLNHFMTEB-UHFFFAOYSA-N 0.000 claims description 2
239000000945 filler Substances 0.000 claims description 2
238000005243 fluidization Methods 0.000 claims description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
239000012948 isocyanate Substances 0.000 claims description 2
239000000049 pigment Substances 0.000 claims description 2
WVWHRXVVAYXKDE-UHFFFAOYSA-N piperine Natural products O=C(C=CC=Cc1ccc2OCOc2c1)C3CCCCN3 WVWHRXVVAYXKDE-UHFFFAOYSA-N 0.000 claims description 2
229920001223 polyethylene glycol Polymers 0.000 claims description 2
230000003068 static effect Effects 0.000 claims description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 2
229920002554 vinyl polymer Polymers 0.000 claims description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims 2
230000000996 additive effect Effects 0.000 claims 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims 2
239000011976 maleic acid Substances 0.000 claims 2
239000012963 UV stabilizer Substances 0.000 claims 1
238000006243 chemical reaction Methods 0.000 abstract description 7
239000000463 material Substances 0.000 abstract description 6
238000006116 polymerization reaction Methods 0.000 abstract description 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 8
239000000428 dust Substances 0.000 description 4
238000001914 filtration Methods 0.000 description 4
238000000227 grinding Methods 0.000 description 4
238000012986 modification Methods 0.000 description 4
230000004048 modification Effects 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
230000000903 blocking effect Effects 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
238000007710 freezing Methods 0.000 description 3
230000008014 freezing Effects 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
ZBRZSJUFJUMKIM-UHFFFAOYSA-N 3-(1-phenylpropan-2-ylamino)propanenitrile;hydrochloride Chemical compound Cl.N#CCCNC(C)CC1=CC=CC=C1 ZBRZSJUFJUMKIM-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
239000008199 coating composition Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000004132 cross linking Methods 0.000 description 2
229940098237 dicel Drugs 0.000 description 2
238000004070 electrodeposition Methods 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
238000005187 foaming Methods 0.000 description 2
239000012046 mixed solvent Substances 0.000 description 2
239000011342 resin composition Substances 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000012360 testing method Methods 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
239000005058 Isophorone diisocyanate Substances 0.000 description 1
RFFFKMOABOFIDF-UHFFFAOYSA-N Pentanenitrile Chemical compound CCCCC#N RFFFKMOABOFIDF-UHFFFAOYSA-N 0.000 description 1
244000137852 Petrea volubilis Species 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
230000003078 antioxidant effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical class C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
238000007664 blowing Methods 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000007547 defect Effects 0.000 description 1
230000002542 deteriorative effect Effects 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000004821 distillation Methods 0.000 description 1
238000009503 electrostatic coating Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
239000000155 melt Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 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
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
239000002245 particle Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
238000010298 pulverizing process Methods 0.000 description 1
238000002310 reflectometry Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000004079 stearyl 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])[H] 0.000 description 1
239000010959 steel Substances 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical class CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
229910000165 zinc phosphate Inorganic materials 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
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
- C08J3/095—Oxygen containing compounds
- 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
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
- 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
- C08J2333/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers
- C08J2333/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Derivatives of such polymers esters

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Dispersion Chemistry (AREA)
General Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

CA002209320A 1997-06-30 1997-06-30 Procede pour la production d'un revetement pulverulent Expired - Fee Related CA2209320C (fr)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
CA002209320A CA2209320C (fr)	1997-06-30	1997-06-30	Procede pour la production d'un revetement pulverulent
GB9714011A GB2326883B (en)	1997-06-30	1997-07-02	Process for production of a powder coating

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CA002209320A CA2209320C (fr)	1997-06-30	1997-06-30	Procede pour la production d'un revetement pulverulent
GB9714011A GB2326883B (en)	1997-06-30	1997-07-02	Process for production of a powder coating

Publications (2)

Publication Number	Publication Date
CA2209320A1 CA2209320A1 (fr)	1998-12-30
CA2209320C true CA2209320C (fr)	2006-07-18

Family

ID=25679457

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002209320A Expired - Fee Related CA2209320C (fr)	1997-06-30	1997-06-30	Procede pour la production d'un revetement pulverulent

Country Status (2)

Country	Link
CA (1)	CA2209320C (fr)
GB (1)	GB2326883B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN103857751A (zh) *	2011-10-07	2014-06-11	东友精细化工有限公司	用于制备取向层的组合物、由其制备的取向层和延迟膜

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3781379A (en) *	1971-08-16	1973-12-25	Ford Motor Co	Powdered coating compositions containing glycidyl methacrylate copolymers with anhydride crosslinking agents and flow control agent
US3942261A (en) *	1973-12-21	1976-03-09	Toyo Ink Manufacturing Co., Ltd.	Method for producing powder paint
JP2774985B2 (ja) *	1991-06-06	1998-07-09	日本ペイント株式会社	粉体塗料用樹脂組成物
WO1996003464A1 (fr) *	1994-07-25	1996-02-08	Kansai Paint Company, Limited	Composition de revetement en poudre thermodurcissable

1997
- 1997-06-30 CA CA002209320A patent/CA2209320C/fr not_active Expired - Fee Related
- 1997-07-02 GB GB9714011A patent/GB2326883B/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
GB2326883B (en)	2001-07-11
GB9714011D0 (en)	1997-09-10
CA2209320A1 (fr)	1998-12-30
GB2326883A (en)	1999-01-06

Legal Events

Date	Code	Title	Description
2002-06-04	EEER	Examination request
2009-06-30	MKLA	Lapsed

Publication	Publication Date	Title
EP0301557B1 (fr)	1992-09-23	Composition de revêtement en poudre thermodurcissable
CA1052494A (fr)	1979-04-10	Produit de revetement en poudre thermodurcissable constitue d'un melange de polymeres de type acrylique a differentes temperatures de transition a l'etat vitreux et a agent reticulant de type polyisocynate protege
DE69700567T2 (de)	2000-05-04	Überzugszusammensetzungen mit fliessreglern, fliessregler und mehrschichtige überzüge
US5998507A (en)	1999-12-07	Thermosetting powder coating material and method
EP1314764B1 (fr)	2005-09-07	Procédé pour la préparation d'une peinture pulvérulente en granules
EP0773267B1 (fr)	1999-12-29	Composition de revetement en poudre thermodurcissable
JP2002506113A5 (fr)	2006-04-20
US5763535A (en)	1998-06-09	Process for production of a powder coating
US6506820B2 (en)	2003-01-14	Method for manufacture of particles for powder coating
US6331581B1 (en)	2001-12-18	Method for color matching of powder coating composition and process for the preparation thereof
CA2209320C (fr)	2006-07-18	Procede pour la production d'un revetement pulverulent
JP2822019B2 (ja)	1998-11-05	粉体塗料用樹脂組成物
US6348520B1 (en)	2002-02-19	Method for color matching of powder coating composition
KR100466043B1 (ko)	2005-07-11	분체도료의제조방법
US20020061957A1 (en)	2002-05-23	Coating composition for undercoat and coating method for repair employing the same
US5908900A (en)	1999-06-01	Elasticity imparting agents for paints, a method of manufacture and paints
JPH1180613A (ja)	1999-03-26	熱硬化性アクリル粉体塗料組成物及びその製造方法
JP2000063705A (ja)	2000-02-29	熱硬化性粉体塗料
JP2004051784A (ja)	2004-02-19	自動車用水性ベース塗料組成物及びこれを用いた複層塗膜形成方法
CN100547008C (zh)	2009-10-07	热固性粉末涂料及其制备方法
JPS5830345B2 (ja)	1983-06-28	熱硬化性粉体塗料組成物
JP2002020692A (ja)	2002-01-23	粉体塗料の製造方法
EP0535667A2 (fr)	1993-04-07	Compositions thermodurcissables, catalyseurs acides thermiquement latents, procédé de revêtement et articles revêtus
JPH06220394A (ja)	1994-08-09	高固形分塗料組成物
JPH1180652A (ja)	1999-03-26	熱硬化性粉体塗料の製造方法