CA2524488A1 - Dual radiation/thermal cured coating composition - Google Patents
Dual radiation/thermal cured coating composition Download PDFInfo
- Publication number
- CA2524488A1 CA2524488A1 CA002524488A CA2524488A CA2524488A1 CA 2524488 A1 CA2524488 A1 CA 2524488A1 CA 002524488 A CA002524488 A CA 002524488A CA 2524488 A CA2524488 A CA 2524488A CA 2524488 A1 CA2524488 A1 CA 2524488A1
- Authority
- CA
- Canada
- Prior art keywords
- coating composition
- component
- radiation
- functional groups
- groups
- Prior art date
- 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.)
- Abandoned
Links
- 239000008199 coating composition Substances 0.000 title claims abstract description 122
- 230000005855 radiation Effects 0.000 title claims abstract description 122
- 230000009977 dual effect Effects 0.000 title description 8
- 125000000524 functional group Chemical group 0.000 claims abstract description 66
- 238000004132 cross linking Methods 0.000 claims abstract description 30
- 239000011230 binding agent Substances 0.000 claims abstract description 27
- 239000003085 diluting agent Substances 0.000 claims abstract description 21
- 229920000642 polymer Polymers 0.000 claims abstract description 10
- 238000000576 coating method Methods 0.000 claims description 52
- -1 cyclic anhydride Chemical class 0.000 claims description 45
- 238000000034 method Methods 0.000 claims description 36
- 229920000728 polyester Polymers 0.000 claims description 30
- 239000011248 coating agent Substances 0.000 claims description 26
- 229920005862 polyol Polymers 0.000 claims description 22
- 150000003077 polyols Chemical class 0.000 claims description 22
- 239000000758 substrate Substances 0.000 claims description 22
- 150000002009 diols Chemical class 0.000 claims description 21
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 20
- 229920000570 polyether Polymers 0.000 claims description 14
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 13
- 229920005906 polyester polyol Polymers 0.000 claims description 11
- 239000012948 isocyanate Substances 0.000 claims description 10
- 150000002513 isocyanates Chemical class 0.000 claims description 10
- 229920003023 plastic Polymers 0.000 claims description 8
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- 229920003180 amino resin Polymers 0.000 claims description 6
- 230000009477 glass transition Effects 0.000 claims description 6
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 5
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 2
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 2
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- 229910000077 silane Inorganic materials 0.000 claims 1
- 239000000049 pigment Substances 0.000 description 59
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate group Chemical group C(C=C)(=O)[O-] NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 24
- 239000000463 material Substances 0.000 description 21
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- 238000001723 curing Methods 0.000 description 16
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- 239000007787 solid Substances 0.000 description 10
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- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 7
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
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- 238000001029 thermal curing Methods 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 5
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 5
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- 238000010894 electron beam technology Methods 0.000 description 5
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- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 5
- 150000002596 lactones Chemical class 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000010445 mica Substances 0.000 description 5
- 229910052618 mica group Inorganic materials 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000454 talc Substances 0.000 description 5
- 229910052623 talc Inorganic materials 0.000 description 5
- 229940113165 trimethylolpropane Drugs 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
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- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical group C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 230000005540 biological transmission Effects 0.000 description 4
- 239000001569 carbon dioxide Substances 0.000 description 4
- 229910002092 carbon dioxide Inorganic materials 0.000 description 4
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- 239000000919 ceramic Substances 0.000 description 4
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- 239000003960 organic solvent Substances 0.000 description 4
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 3
- IZSHZLKNFQAAKX-UHFFFAOYSA-N 5-cyclopenta-2,4-dien-1-ylcyclopenta-1,3-diene Chemical group C1=CC=CC1C1C=CC=C1 IZSHZLKNFQAAKX-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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- 239000007983 Tris buffer Substances 0.000 description 3
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- 125000004432 carbon atom Chemical group C* 0.000 description 3
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 3
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- 150000002334 glycols Chemical class 0.000 description 3
- HNMCSUXJLGGQFO-UHFFFAOYSA-N hexaaluminum;hexasodium;tetrathietane;hexasilicate Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].S1SSS1.S1SSS1.[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] HNMCSUXJLGGQFO-UHFFFAOYSA-N 0.000 description 3
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 3
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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
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
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Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
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| DE19939760A1 (de) * | 1999-08-21 | 2001-03-08 | Schenectady Int Inc | Verfahren und Vorrichtung zur Isolierung elektrotechnischer Bauteile |
| DE10113884B4 (de) * | 2001-03-21 | 2005-06-02 | Basf Coatings Ag | Verfahren zum Beschichten mikroporöser Oberflächen und Verwendung des Verfahrens |
| DE10115505B4 (de) * | 2001-03-29 | 2007-03-08 | Basf Coatings Ag | Thermisch und mit aktinischer Strahlung härtbare wäßrige Dispersionen, Verfahren zu ihrer Herstellung und ihre Verwendung |
| WO2005078030A2 (en) * | 2004-02-11 | 2005-08-25 | E.I. Dupont De Nemours And Company | Near infrared radiation curable powder coating composition having enhanced flow characteristics |
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| US20060088720A1 (en) * | 2004-10-22 | 2006-04-27 | Niederst Ken W | Coated packaging materials |
| EP1879938B1 (en) * | 2005-05-02 | 2012-04-18 | Cytec Surface Specialties, S.A. | Radiation curable urethane (meth)acrylate polymer and adhesives formulated with them |
| US7713628B2 (en) * | 2005-05-31 | 2010-05-11 | Chemque, Inc. | Actinic radiation curable coating compositions |
| US20070066698A1 (en) * | 2005-09-20 | 2007-03-22 | Yang Wenliang P | Dual cure compositions, methods of curing thereof and articles therefrom |
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| US20070212553A1 (en) * | 2006-03-10 | 2007-09-13 | Stearns Robert B | Puncture resistant composite |
| US20070231577A1 (en) * | 2006-03-30 | 2007-10-04 | Basf Corporation | Coatings for polycarbonate windows |
| US9080061B2 (en) * | 2006-05-03 | 2015-07-14 | Surface Solutions Laboratories | Coating resins and coating with multiple crosslink functionalities |
| US20080107564A1 (en) | 2006-07-20 | 2008-05-08 | Shmuel Sternberg | Medical fluid access site with antiseptic indicator |
| US20080039542A1 (en) * | 2006-08-11 | 2008-02-14 | General Electric Company | Composition and associated method |
| TW200811237A (en) * | 2006-08-11 | 2008-03-01 | Momentive Performance Mat Inc | Composition, associated method and article |
| US20090306277A1 (en) * | 2006-08-29 | 2009-12-10 | Goenner Emily S | Resin systems including reactive surface-modified nanoparticles |
| JP5118389B2 (ja) * | 2007-05-26 | 2013-01-16 | 中村製作所株式会社 | ワークへの凹所形成方法 |
| US9125973B2 (en) | 2007-07-20 | 2015-09-08 | Baxter International Inc. | Antimicrobial housing and cover for a medical device |
| USRE47452E1 (en) | 2007-07-20 | 2019-06-25 | Baxter International Inc. | Antimicrobial housing and cover for a medical device |
| US20090155485A1 (en) * | 2007-12-18 | 2009-06-18 | Hoyle Charles E | Rapid curing wood putty based on frontal polymerization |
| US20090169872A1 (en) * | 2007-12-27 | 2009-07-02 | Baxter International Inc. | Radiation curable coatings |
| DE102008008779A1 (de) * | 2008-02-12 | 2009-08-13 | Basf Coatings Ag | Wässriger Beschichtungsstoff, Verfahren zu seiner Herstellung und seine Verwendung |
| US8753561B2 (en) * | 2008-06-20 | 2014-06-17 | Baxter International Inc. | Methods for processing substrates comprising metallic nanoparticles |
| US8178120B2 (en) * | 2008-06-20 | 2012-05-15 | Baxter International Inc. | Methods for processing substrates having an antimicrobial coating |
| US8277826B2 (en) * | 2008-06-25 | 2012-10-02 | Baxter International Inc. | Methods for making antimicrobial resins |
| US20090324738A1 (en) * | 2008-06-30 | 2009-12-31 | Baxter International Inc. | Methods for making antimicrobial coatings |
| US20100227052A1 (en) * | 2009-03-09 | 2010-09-09 | Baxter International Inc. | Methods for processing substrates having an antimicrobial coating |
| WO2010121978A1 (de) * | 2009-04-22 | 2010-10-28 | Basf Se | Strahlungshärtbare beschichtungsmassen |
| US9695264B2 (en) * | 2010-04-01 | 2017-07-04 | Ppg Industries Ohio, Inc. | High functionality polyesters and coatings comprising the same |
| US20120138223A1 (en) | 2011-09-29 | 2012-06-07 | General Electric Company | Uv-ir combination curing system and method of use for wind blade manufacture and repair |
| KR101313441B1 (ko) * | 2011-10-25 | 2013-10-01 | 주식회사 포스코 | 용접성, 내스크래치성 및 내식성이 우수한 표면처리 강판 |
| JP5921986B2 (ja) * | 2012-08-10 | 2016-05-24 | ハリマ化成株式会社 | 二液硬化型被覆剤 |
| DE102012015924A1 (de) | 2012-08-10 | 2014-02-13 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Herstellung einer Klebeverbindung oder eines Verbundwerkstoffes und dafür geeigneter Klebe- oder Matrixwerkstoff |
| EP3034569B1 (de) * | 2014-12-19 | 2016-11-30 | Evonik Degussa GmbH | Thermisch nachhärtende mit aktinischer Strahlung vernetzende Systeme |
| KR101674766B1 (ko) * | 2014-12-23 | 2016-11-10 | 주식회사 포스코 | 투명 패턴 프린트 강판 제조 방법 |
| EP3371232B1 (en) | 2015-11-03 | 2021-01-06 | LORD Corporation | Two-parts adhesive system |
| JP6755525B2 (ja) * | 2016-02-19 | 2020-09-16 | 東洋紡株式会社 | 紫外線硬化型塗料の塗工方法および紫外線硬化膜の製造方法 |
| DK3515958T3 (da) * | 2016-09-20 | 2020-09-14 | Covestro Deutschland Ag | Anisotrope kompositmaterialer baseret på polyisocyanater |
| TWI758312B (zh) | 2016-10-26 | 2022-03-21 | 美商3M新設資產公司 | 可交聯組成物及經交聯組成物、包含其之物品及製備物品之方法 |
| KR20190079956A (ko) * | 2017-12-28 | 2019-07-08 | 에스케이씨 주식회사 | 광학 재료용 중합성 조성물 |
| EP3546505B1 (en) | 2018-03-30 | 2021-02-24 | Avery Dennison Corporation | Multilayer coating for covering vehicle body parts |
Family Cites Families (97)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US83397A (en) * | 1868-10-27 | Improvement in billiard-cues | ||
| US77394A (en) * | 1868-04-28 | Improvement in gobi-harvesters | ||
| US78315A (en) * | 1868-05-26 | Improvement in cooking-shoves | ||
| US78316A (en) * | 1868-05-26 | Improved shipping-case | ||
| US4025407A (en) | 1971-05-05 | 1977-05-24 | Ppg Industries, Inc. | Method for preparing high solids films employing a plurality of curing mechanisms |
| DE2259360C2 (de) | 1972-12-04 | 1982-06-09 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Herstellung von dünnen Schichten auf Basis von Polyurethan-Elastomeren |
| US4139385A (en) | 1975-06-20 | 1979-02-13 | General Electric Company | Coating method and composition using cationic photoinitiators polythio components and polyolefin components |
| JPS534048A (en) | 1975-12-26 | 1978-01-14 | Dainippon Toryo Co Ltd | Method of forming multi-layer coating film |
| DE2636425A1 (de) | 1976-08-13 | 1978-02-16 | Basf Ag | Haertbare ueberzugsmassen |
| US4342793A (en) | 1977-01-14 | 1982-08-03 | Henkel Corporation | Interpenetrating dual cure resin compositions |
| US4128600A (en) | 1977-01-14 | 1978-12-05 | General Mills Chemicals, Inc. | Interpenetrating dual cure resin compositions |
| US4247578A (en) | 1977-01-14 | 1981-01-27 | Henkel Corporation | Interpenetrating dual cure resin compositions |
| NL7707669A (nl) | 1977-07-08 | 1979-01-10 | Akzo Nv | Werkwijze voor het bekleden van een substraat met een stralingshardbare bekledingscompositie. |
| US4192762A (en) | 1978-04-20 | 1980-03-11 | Union Carbide Corporation | Radiation curable urethane compositions |
| US4287116A (en) | 1979-05-22 | 1981-09-01 | Ici Americas Inc. | Polyester urethane-containing molding compositions |
| US4675234A (en) | 1980-10-01 | 1987-06-23 | Tarkett Ab | Radiation cured coating and process therefor |
| US4377457A (en) | 1980-11-21 | 1983-03-22 | Freeman Chemical Corporation | Dual cure coating compositions |
| US4481093A (en) | 1981-10-13 | 1984-11-06 | Desoto, Inc. | Ultraviolet curable basecoats for vacuum metallization |
| US4415604A (en) | 1982-11-12 | 1983-11-15 | Loctite Corporation | Conformal coating and potting system |
| US4424252A (en) | 1982-11-12 | 1984-01-03 | Loctite Corporation | Conformal coating systems |
| US4532021A (en) | 1983-07-18 | 1985-07-30 | Desoto, Inc. | Adherent ultraviolet cured coatings |
| US4526939A (en) | 1983-07-18 | 1985-07-02 | Desoto, Inc. | Thermosetting coating compositions for the sealing of fiber reinforced plastics |
| DE3407087C2 (de) | 1984-02-27 | 1994-07-07 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V., 8000 München | Verfahren und Lack zur Herstellung von kratzfesten Beschichtungen |
| US4607084A (en) | 1984-06-11 | 1986-08-19 | Celanese Specialty Resins, Inc. | Radiation curable acrylated polyurethane oligomer compositions |
| US4618632A (en) | 1985-02-07 | 1986-10-21 | Westinghouse Electric Corp. | UV curable high tensile strength resin composition |
| US4634602A (en) * | 1986-01-02 | 1987-01-06 | Ppg Industries, Inc. | Primer composition |
| US4761435A (en) | 1986-10-03 | 1988-08-02 | Desoto, Inc. | Polyamine-polyene ultraviolet coatings |
| US5089376A (en) | 1986-12-08 | 1992-02-18 | Armstrong World Industries, Inc. | Photoimagable solder mask coating |
| US4786657A (en) | 1987-07-02 | 1988-11-22 | Minnesota Mining And Manufacturing Company | Polyurethanes and polyurethane/polyureas crosslinked using 2-glyceryl acrylate or 2-glyceryl methacrylate |
| US4952612A (en) | 1987-08-28 | 1990-08-28 | Minnesota Mining And Manufacturing Company | Energy-induced curable compositions |
| US4950696A (en) | 1987-08-28 | 1990-08-21 | Minnesota Mining And Manufacturing Company | Energy-induced dual curable compositions |
| US4985340A (en) | 1988-06-01 | 1991-01-15 | Minnesota Mining And Manufacturing Company | Energy curable compositions: two component curing agents |
| DE3828098A1 (de) | 1988-08-18 | 1990-03-08 | Fraunhofer Ges Forschung | Verfahren und zusammensetzung zur herstellung von kratzfesten materialien |
| US5013631A (en) | 1989-03-03 | 1991-05-07 | Westinghouse Electric Corp. | Ultraviolet curable conformal coatings |
| EP0401892A3 (en) | 1989-06-09 | 1991-08-07 | Akzo N.V. | Thermosetting polyester alloys and coating compositions therefrom |
| DE59009431D1 (de) | 1989-06-16 | 1995-08-31 | Ciba Geigy Ag | Photoresist. |
| DE4011045A1 (de) | 1990-04-05 | 1991-10-10 | Fraunhofer Ges Forschung | Verfahren zum beschichten von kunststoffsubstraten und lack zur verwendung in diesem verfahren |
| DE4020316B4 (de) | 1990-06-26 | 2004-07-08 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Verfahren zur Herstellung eines Lacks und dessen Verwendung |
| DE4025215C2 (de) | 1990-08-09 | 1994-03-10 | Fraunhofer Ges Forschung | Verfahren zur Herstellung eines Lacks und seine Verwendung zum Beschichten von Substraten mit einem alkalistabilen und abriebbeständigen Überzug |
| CA2048232A1 (en) | 1990-09-05 | 1992-03-06 | Jerry W. Williams | Energy curable pressure-sensitive compositions |
| WO1992020719A1 (en) | 1991-05-15 | 1992-11-26 | Sokol Andrew A | Finishing composition which is curable by uv light and method of using same |
| DE4119857A1 (de) | 1991-06-17 | 1992-12-24 | Basf Lacke & Farben | Ueberzugsmittel auf der basis von carboxylgruppenhaltigen polymeren und epoxidharzen |
| DE4122266A1 (de) | 1991-07-05 | 1993-01-07 | Hoechst Ag | Polyurethan-dispersionen |
| DE4122743C1 (enExample) | 1991-07-10 | 1992-11-26 | Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung Ev, 8000 Muenchen, De | |
| US5234970A (en) | 1991-07-16 | 1993-08-10 | W. R. Grace & Co.-Conn. | Dual curing composition based on isocyanate trimer and use thereof |
| DE4133290A1 (de) | 1991-10-08 | 1993-04-15 | Herberts Gmbh | Verfahren zur herstellung von mehrschichtlackierungen unter verwendung von radikalisch und/oder kationisch polymerisierbaren klarlacken |
| DE4209035A1 (de) * | 1992-03-20 | 1993-09-23 | Bayer Ag | Verfahren zur herstellung von hydroxyfunktionellen copolymerisaten |
| DE4215070A1 (de) * | 1992-05-07 | 1993-11-11 | Herberts Gmbh | Verfahren zur Herstellung von Mehrschichtlackierungen |
| DE4222194A1 (de) | 1992-07-07 | 1994-01-13 | Basf Lacke & Farben | Verfahren zur Herstellung einer zweischichtigen Lackierung und für dieses Verfahren geeignete Pulverlacke |
| US5605965A (en) | 1992-10-23 | 1997-02-25 | Basf Corporation | High gloss and/or high DOI coating utilizing carbamate-functional polymer composition |
| US5300328A (en) | 1992-10-23 | 1994-04-05 | Basf Corporation | Partially-defunctionalized aminoplast curing for polymer compositions |
| ZA937635B (en) | 1992-10-23 | 1994-05-05 | Basf Corp | Curable carbamate-functional polymer composition |
| US5356669A (en) | 1992-10-23 | 1994-10-18 | Basf Corporation | Composite color-plus-clear coating utilizing carbamate-functional polymer composition in the clearcoat |
| US6103816A (en) | 1992-10-30 | 2000-08-15 | Ppg Industries Ohio, Inc. | Aqueous aminoplast curable film-forming compositions providing films having resistance to acid etching |
| BR9307434A (pt) | 1992-10-30 | 1999-06-01 | Ppg Industries Inc | Composição formadora de película carável |
| US5610224A (en) | 1992-10-30 | 1997-03-11 | Basf Corporation | Water dispersible ionic and nonionic polyamide modified polyurethane resins for use in coating composition |
| TW242644B (enExample) | 1992-10-30 | 1995-03-11 | Ppg Industries Inc | |
| US5409740A (en) | 1992-12-18 | 1995-04-25 | Lord Corporation | Dual-cure method of forming industrial threads |
| DE4302327A1 (de) | 1993-01-28 | 1994-08-04 | Basf Lacke & Farben | Strahlenhärtbare Oligomere sowie flüssige, strahlenhärtbare Überzugsmasse für die Beschichtung von Glasoberflächen |
| FR2701268B1 (fr) | 1993-02-05 | 1995-04-14 | Atochem Elf Sa | Peintures à base de poudres de polyamide destinées au revêtement de profilés PVC. |
| US6534187B2 (en) | 1993-02-08 | 2003-03-18 | Fraunhofer-Gesellschaft Zur Foerderung Der Angewandten Forschung E.V. | Coating material and process for the production of functional coatings |
| DE4310414A1 (de) | 1993-03-31 | 1994-10-06 | Basf Lacke & Farben | Verfahren zur Herstellung einer zweischichtigen Decklackierung auf einer Substratoberfläche |
| AU719294B2 (en) | 1995-05-19 | 2000-05-04 | Basf Coatings Aktiengesellschaft | Aqueous powder coating dispersion |
| IT1276480B1 (it) | 1995-07-07 | 1997-10-31 | Fiat Auto Spa | Metodo di verniciatura migliorato applicabile su elementi in materiale plastico, in particolare componenti automobilistici in |
| US5965213A (en) | 1996-04-04 | 1999-10-12 | Basf Coatings Ag | Aqueous dispersions of a transparent powder coating |
| US5891961A (en) * | 1996-05-07 | 1999-04-06 | Kansai Paint Co., Ltd | Coating composition and coating method |
| WO1998020047A1 (en) | 1996-11-07 | 1998-05-14 | H.B. Fuller Licensing & Financing, Inc. | Isocyanates as reactive diluents in the preparation of polymers |
| US5922473A (en) | 1996-12-26 | 1999-07-13 | Morton International, Inc. | Dual thermal and ultraviolet curable powder coatings |
| DE19709560C1 (de) | 1997-03-07 | 1998-05-07 | Herberts Gmbh | Überzugsmittel zur Mehrschichtlackierung und Verwendung der Überzugsmittel in einem Verfahren zur Lackierung |
| WO1998045344A1 (en) | 1997-04-08 | 1998-10-15 | Dsm N.V. | Radiation-curable binder compositions having high elongation and toughness after cure |
| DE19715382C1 (de) | 1997-04-14 | 1998-11-19 | Synthopol Chemie Dr Koch | Wasserdispergierte, strahlenhärtbare Polyurethane |
| DE19716020A1 (de) | 1997-04-17 | 1998-10-22 | Basf Ag | Dispersionen enthaltend ein Polyurethan und ein strahlenhärtbares Präpolymer |
| DE19826715A1 (de) | 1997-07-21 | 1999-01-28 | Basf Ag | Strahlungshärtbare Verbindungen auf Basis von 2,4-Diethyloctandiol |
| US6177535B1 (en) | 1997-09-22 | 2001-01-23 | Basf Aktiengesellchaft | Preparing radiation-curable, urethane-functional prepolymers |
| DE19853813A1 (de) | 1997-12-10 | 1999-06-17 | Henkel Kgaa | Klebstoff mit mehrstufiger Aushärtung und dessen Verwendung bei der Herstellung von Verbundmaterialien |
| EP0939091A1 (en) | 1998-02-27 | 1999-09-01 | Basf Corporation | An extremely fast curing chemical reactive coating composition, which may cure at ambient or low temperatures, with long useable pot life |
| DE19809643B4 (de) | 1998-03-06 | 2004-04-08 | Basf Coatings Ag | Beschichtungsmittel und Klebstoffe, ihre Verwendung und Verfahren zu ihrer Herstellung |
| US6344501B1 (en) | 1998-04-01 | 2002-02-05 | Basf Coatings Ag | Non-ionically stabilized transparent powder-coating dispersion |
| DE19814872A1 (de) | 1998-04-02 | 1999-10-07 | Basf Ag | Strahlungshärtbare Zubereitungen |
| DE19818735A1 (de) | 1998-04-27 | 1999-10-28 | Herberts Gmbh | Strahlungshärtbare Beschichtungsmittel und deren Verwendung |
| DE19855116A1 (de) | 1998-11-30 | 2000-05-31 | Basf Coatings Ag | Bautenanstrichstoff, Verfahren zu seiner Herstellung und seine Verwendung |
| DE19920799A1 (de) | 1999-05-06 | 2000-11-16 | Basf Coatings Ag | Thermisch und mit aktinischer Strahlung härtbarer Beschichtungsstoff und seine Verwendung |
| DE19920801A1 (de) | 1999-05-06 | 2000-11-16 | Basf Coatings Ag | Hochkratzfeste mehrschichtige Lackierung, Verfahren zu ihrer Herstellung und ihre Verwendung |
| DE19924674C2 (de) | 1999-05-29 | 2001-06-28 | Basf Coatings Ag | Thermisch und mit aktinischer Strahlung härtbarer Beschichtungsstoff und seine Verwendung |
| DE19930067A1 (de) | 1999-06-30 | 2001-01-11 | Basf Coatings Ag | Beschichtungsstoff und seine Verwendung zur Herstellung von Füllerschichten und Steinschlagschutzgrundierungen |
| DE19930664A1 (de) | 1999-07-02 | 2001-01-11 | Basf Coatings Ag | Klarlack und seine Verwendung zur Herstellung von Klarlackierungen und farb- und/oder effektgebenden Mehrschichtlackierungen |
| DE19930665A1 (de) | 1999-07-02 | 2001-01-11 | Basf Coatings Ag | Basislack und seine Verwendung zur Herstellung von farb- und/oder effektgebenden Basislackierungen und Mehrschichtlackierung |
| DE10004498A1 (de) | 2000-02-02 | 2001-08-09 | Basf Coatings Ag | Diethyloctandioldicarbamate und Diethyloctandioldiallophanate, Verfahren zu ihrer Herstellung und ihre Verwendung |
| MXPA03000930A (es) | 2000-07-31 | 2003-10-06 | Ppg Ind Ohio Inc | Composiciones duales de revestimiento curadas que tienen resistencia mejorada al resquebrajamiento, substratos revestidos y metodos relacionados con lo mismo. |
| CN1286874C (zh) | 2000-10-25 | 2006-11-29 | 阿克佐诺贝尔股份有限公司 | 光敏水性涂料组合物 |
| DE10113884B4 (de) * | 2001-03-21 | 2005-06-02 | Basf Coatings Ag | Verfahren zum Beschichten mikroporöser Oberflächen und Verwendung des Verfahrens |
| DE10115604A1 (de) * | 2001-03-29 | 2002-10-10 | Basf Coatings Ag | Thermisch und mit aktinischer Strahlung härtbares Gemisch und seine Verwendung |
| JP4633952B2 (ja) * | 2001-03-30 | 2011-02-16 | 関西ペイント株式会社 | 塗膜形成方法 |
| US20030077394A1 (en) | 2001-08-28 | 2003-04-24 | Bradford Christophen J. | Dual cure coating composition and process for using the same |
| US20030078315A1 (en) | 2001-08-28 | 2003-04-24 | Bradford Christopher J. | Dual cure coating composition and processes for using the same |
| US20030083397A1 (en) | 2001-08-28 | 2003-05-01 | Bradford Christopher J. | Dual cure coating composition and process for using the same |
| US6835759B2 (en) | 2001-08-28 | 2004-12-28 | Basf Corporation | Dual cure coating composition and processes for using the same |
-
2003
- 2003-06-04 US US10/454,056 patent/US6852771B2/en not_active Expired - Lifetime
-
2004
- 2004-04-14 MX MXPA05012868 patent/MX249623B/es active IP Right Grant
- 2004-04-14 WO PCT/US2004/011418 patent/WO2004108844A2/en not_active Ceased
- 2004-04-14 JP JP2006509999A patent/JP2006526688A/ja active Pending
- 2004-04-14 EP EP04785674A patent/EP1629056A2/en not_active Withdrawn
- 2004-04-14 CA CA002524488A patent/CA2524488A1/en not_active Abandoned
- 2004-04-14 BR BRPI0410987-2A patent/BRPI0410987A/pt not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| MX249623B (es) | 2007-09-28 |
| US6852771B2 (en) | 2005-02-08 |
| US20030207956A1 (en) | 2003-11-06 |
| BRPI0410987A (pt) | 2006-07-04 |
| WO2004108844A3 (en) | 2005-06-09 |
| EP1629056A2 (en) | 2006-03-01 |
| JP2006526688A (ja) | 2006-11-24 |
| WO2004108844A2 (en) | 2004-12-16 |
| MXPA05012868A (es) | 2006-02-22 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |