WO1993023447A1 - Binder composition for powder coatings for use as a top coat in the automotive industry and top-coated automotive substrates - Google Patents

Binder composition for powder coatings for use as a top coat in the automotive industry and top-coated automotive substrates Download PDF

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Publication number
WO1993023447A1
WO1993023447A1 PCT/NL1993/000097 NL9300097W WO9323447A1 WO 1993023447 A1 WO1993023447 A1 WO 1993023447A1 NL 9300097 W NL9300097 W NL 9300097W WO 9323447 A1 WO9323447 A1 WO 9323447A1
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WO
WIPO (PCT)
Prior art keywords
resin
koh
binder composition
acid
polyester
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.)
Ceased
Application number
PCT/NL1993/000097
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English (en)
French (fr)
Inventor
Franciscus Maria Witte
Gerrit Kieft
Wilhelmus Henricus Antonius Van Den Elshout
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.)
Koninklijke DSM NV
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.)
Filing date
Publication date
Application filed by DSM NV filed Critical DSM NV
Priority to DE69309459T priority Critical patent/DE69309459T2/de
Priority to EP93913622A priority patent/EP0640106B1/en
Priority to US08/335,884 priority patent/US5580660A/en
Publication of WO1993023447A1 publication Critical patent/WO1993023447A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4205—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups
    • C08G18/4208—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups
    • C08G18/4211—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols
    • C08G18/4219—Polycondensates having carboxylic or carbonic ester groups in the main chain containing cyclic groups containing aromatic groups derived from aromatic dicarboxylic acids and dialcohols from aromatic dicarboxylic acids and dialcohols in combination with polycarboxylic acids and/or polyhydroxy compounds which are at least trifunctional
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
    • C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
    • C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
    • C08G18/6225—Polymers of esters of acrylic or methacrylic acid
    • C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78—Nitrogen
    • C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72—Polyisocyanates or polyisothiocyanates
    • C08G18/80—Masked polyisocyanates
    • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
    • C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
    • C08G18/808—Monoamines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2150/00—Compositions for coatings
    • C08G2150/20—Compositions for powder coatings
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31547—Of polyisocyanurate
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31605—Next to free metal

Definitions

  • the invention relates to a binder composition for powder coatings for use a top coat in the automotive industry.
  • the invention also concerns top-coated automotive substrates.
  • the top coat or finish coat is the coating intended to be the last coat applied in a coating system and is usually applied over a primer, a basecoat or surfaces.
  • the clear top coats which, according to the present state of the art in the automotive industry, are used as a two-component system are solvent-containing paint systems based on acrylate resins cured with isocyanates. In order to meet the requirements regarding the reduction in solvent emissions, so-called high-solids systems are already being used. The only way to reduce solvent emissions still further is to use powder coatings for clear automotive coatings (Lattice, E. "Pulverlack am Auto; Aus der reform der Autoindustrie", presented at "Der Pulver Economics ' 92 , 23.01.92, M ⁇ nchen”; JOT-Verbeck, pages 1-11).
  • the binder composition according to the invention comprises a polyester containing hydroxyl groups having a hydroxyl number of between 20 and 100 mg KOH/g resin and an acid number of less than 10 mg KOH/g resin or a polyacrylate containing hydroxyl groups having a hydroxyl number between 40 and 150 mg KOH/g resin and an acid number of less than 20 mg KOH/g resin and a blocked hexamethylenedusocyanate trimer.
  • the binder composition according to the invention results in powder coatings with optimum flow, gasoline resistance, flexibility and clarity at a curing temperature of between 130°C and 170°C.
  • the isocyanate trimer is blocked with 1,2,4- triazole.
  • the weight ratio of the polymer containing hydroxyl groups to the blocked hexamethylenedusocyanate trimer is usually between 90:10 and 50:50. Said ratio is amongst others depending of the hydroxyl number of the polymer.
  • the binder composition can also comprise mixtures of hydroxyl-functional polyesters and hydroxyl-functional polyacrylates.
  • the hydroxyl functional polymers are mixed with the blocked crosslinker at a temperature of approximately 100°C by means of, for example, extrusion, and after being electrostatically sprayed the mixture can be cured at temperatures of between 130°C and 170°C, preferably at or below 150°C.
  • the usual additives such as fillers, flow aids and/or stabilizers and also pigments if desired, can be added to the coating systems, preferably during extrusion.
  • Suitable polyesters can be obtained by the usual preparation methods from mainly aromatic polycarboxylic acids.
  • Suitable acids include phthalic acid, isophthalic acid, terephthalic acid, pyro ellitic acid, trimellitic acid, 3,6-dichlorophthalic acid, tetrachlorophthalic acid and, if available, the anhydrides, acid chlorides or lower alkylesters of these.
  • the carboxylic acid component often consists of at least 50 wt%, preferably at least 70 mol%, isophthalic acid and/or terephthalic acid.
  • polyols such as glycerol, hexane- triol, pentaery
  • Epoxy compounds can also be used instead of diols or polyols.
  • the alcohol component preferably contains at least 50 mol% neopentylglycol.
  • Neopentylglycol and/or trimethylolpropane are preferably used as polyols.
  • a powder coating composition according to the present invention, in which the polyester component thereof was made using these polyols, will yield a coating having good outdoor durability.
  • Suitable polycarboxylic acids include cyclo- aliphatic and/or acyclic polycarboxylic acids such as, for example cyclohexane dicarboxylic acid, tetrahydrophthalic acid, hexahydroendomethylenetetrahydrophthalic acid, azelaic acid, sebacic acid, decane dicarboxylic acid, fatty acid dimer, adipic acid, succinic acid and maleic acid. Normally they will be used in amounts up to at the most 30 mol%, preferably up to a maximum of 20 mol% of the total carboxylic acid.
  • Hydroxycarboxylic acids and/or possibly lactones can also be used, such as for example 12-hydroxyl- stearic acid, ⁇ -caprolactone and hydroxypivalic acid ester of neopentylglycol.
  • monocarboxylic acids such as benzoic acid, tert.-butylbenzoic acid, hexahydro- benzoic acid and saturated aliphatic monocarboxylic acids can also be added in the preparation.
  • the polyesters are prepared using methods known per se by esterification or transeste ification, possibly in the presence of the usual catalysts such as for example dibutyl tin oxide or terabutyl titanate.
  • a suitable choice of preparation conditions and of COOH/OH ratio result in a resin with a hydroxyl number of between 20 and 100 mg KOH/g resin and an acid number of less than 10 mg KOH/g resin.
  • the polyester is based on 40-100 mol% isophthalic acid and 0-60% terephthalic acid as dicarboxylic acids (the amounts of isophthalic acid and terephthalic acid together making 100 mol%). More preferably the amount of isophthalic acid is higher than 60 mol%.
  • the polyester can also be based on more than two dicarboxylic acids.
  • the amount of monomer with a functionality of three or more is preferably lower than 12% of the other monomers.
  • the number-average molecular weight (Mn) is preferably between . 1,500 and 5,000.
  • the molecular weight combined with the amount of branching component is preferably chosen so that the functionality of the polyester is between 2.0 and 4.0.
  • the hydroxyl-functional acrylate resin is usually based on hydroxyethyl(meth)acrylate, hydroxypropyl(meth)- acrylate and methyl(meth)acrylate.
  • the resin can also be based on (meth)acrylic acid and alkyl esters of (meth)- acrylic acid such as for example ethyl(meth)acrylate, isopropyl(meth)acrylate, n-butyl(meth)acrylate, n-propyl- (meth)acrylate, isobutyl(meth)acrylate, ethylhexylacrylate and/or cyclohexyl(meth)acrylate and vinyl compounds such as for example styrene.
  • Hydroxyl-functional acrylate resins can be prepare by polymerization, the first step being the addition of a solvent, for example toluene, xylene or butyl acetate, to the reactor. This is then heated to the temperature at whic the solvent boils, following which monomers, initiator and possibly mercaptan are added for a period of for example between two and four hours. The temperature is then kept at reflux temperature for for example two hours. The solvent i then distilled off by means of a temperature increase followed by vacuum distillation for for example from one to two hours. After this the product is drained and cooled.
  • a solvent for example toluene, xylene or butyl acetate
  • EP-A-4571 describes the use of 1,2,4-triazole blocked isocyanates in powder and solvent based lacquers based on hydroxyl-functional polymers. EP-A-4571 does not, however, give any indication that the stated problem in the automotive industry can be solved with the specific binder composition according to the present invention.
  • US-A-4748242 discloses a process for the production of polyisocyanates containing isocyanurate groups by trimerizing a mixture of aliphatic-cycloaliphatic diisocyanates having a sterically unhindered isocyanate group bound to a primary aliphatic carbon atom and a sterically hindered isocyanate group bound to a tertiary carbon atom which forms a part of a cycloaliphatic ring system and 1,6-diisocyanatohexane.
  • the patent is also directed to the polyisocyanates containing isocyanurate groups produced according to this process and to their use, optionally in blocked form, as an isocyanate component in the production of polyisocyanate polyaddition products, preferably polyurethane lacquers.
  • a suitable blocking agent includes 1,2,4-triazole.
  • an optionally blocked polyisocyanate, poly- functional reaction partner, catalyst and optionally other conventional additives such as pigments are mixed with each other and homogenized on a conventional mixing assembly either with or without solvent and diluent. They can then be applied to the object to be coated in solution or from the melt, or in solid form according to conventional methods.
  • US-A-4748242 does not give any indication that the process result in powder coatings which can be used as clear top coats on exterior parts in automotive industry.
  • Novel top-coated automobile parts comprise a substrate, e.g. a body panel or work or other automobile parts (such as for example wheels, wheelcovers and doors), having, if desired, a pigment layer or layers thereon and a clear top coat over the pigment layer or layers (if present) wherein the top coat comprises a solvent-free powder coating based on the present binder composition.
  • the powder coatings obtained with the binder compositions according to the invention can also be used on wood or plastic, as well as vehicle parts such as body parts, such as wheels, wheelcovers, fenders, doors, hoods and the like.
  • the powder coatings of the present invention are also useful or industrial top coats for general purposes, for top coats for machinery and equipment, especially top coats for metal, for example cans, household articles and other small pieces of equipment.
  • Table 2 shows the hydroxyl number (mg KOH/g resin), the viscosity measured with the Emila rheometer (in dPa.s, 165 °C) and the glass transition temperature (Tg, Mettler TA-3000 system 5°C/min).
  • IPA isophthalic acid
  • NPG neopentylglycol
  • a 6-litre reactor vessel fitted with a thermometer, an agitator and a reflux cooler was filled with 1,500 g of toluene. With stirring, while a light nitrogen stream was fed over the reaction mixture, the temperature was then raised to reflux temperature.
  • the monomer mixture comprising a total of 3,000 g of monomers (in the ratio as given in Table 3) the given amount of initiator (Luperox 575TM; Atochem) was dissolved. This mixture was then added to the reactor in 3 hours. The temperature in the reactor was kept at the reflux temperature. Two hours after the addition of the monomer mixture a separator tank was included in the set-up and the solvent was removed by means of an increase in temperature and the creation of a vacuum.
  • Table 3 gives the monomer ratio in weight percentages, the viscosity measured using the Emila rheometer (in dPa.s, 165°C) and the glass transition temperature (Tg, Mettler TA-3000, system 5°C/min).
  • MMA methylmethacrylate
  • BA butylmethacrylate
  • Experiment I was repeated with, as polyester resin, 495 g of polyester according to Experiment 2, 105 g of crosslinker according to Experiment 6, 4 g of BYKTM 361 and 2 g of benzoin being used.
  • Experiment I was repeated with, as polyester resin, 453 g of polyester according to Experiment 3, 147 g of crosslinker according to Experiment 6, 4 g of BYKTM 361 and 2 g of benzoin being used.
  • the powder coatings obtained using Examples I-V were judged visually as to their exterior appearance, their clarity and their flow.
  • the gasoline resistance was determined by placing a wad of cotton wool soaked in gasoline on the coating for 2 hours under a slide, and then visually assessing any attack on the coating.
  • Mechanical properties were determined using the "Erichsen slow penetration test” (in accordance with ISO-1520/DIN 53156) and the “reverse impact test” (in accordance with ASTM-2794/69) .
  • a top coating for exterior automotive applications comprising a powder coating obtained from the above-described polyester resins and acrylate resins plus cross-linker is curable at acceptable and relatively low curing temperatures, and exhibits the highly desired combination of good flow, clarity, gasoline resistance and flexibility.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Adhesives Or Adhesive Processes (AREA)
PCT/NL1993/000097 1992-05-15 1993-05-12 Binder composition for powder coatings for use as a top coat in the automotive industry and top-coated automotive substrates Ceased WO1993023447A1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
DE69309459T DE69309459T2 (de) 1992-05-15 1993-05-12 Verwendung einer bindemittelzusammensetzung für die herstellung von als deckschicht im pkw-bereich verwendbaren pulverlacken und mit dieser deckschicht beschichtete pkw-gegenstände
EP93913622A EP0640106B1 (en) 1992-05-15 1993-05-12 Use of a binder composition for the preparation of powder coatings for use as top coat in the automotive industry and top-coated automotive substrates
US08/335,884 US5580660A (en) 1992-05-15 1993-05-12 Use of a binder composition for the preparation of a powder coating for use as a top coat in the automotive industry and top-coated automotive substrates

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
BE9200451 1992-05-15
BE9200451A BE1005819A3 (nl) 1992-05-15 1992-05-15 Bindmiddelsamenstelling voor poedercoatings toepasbaar in de automobielindustrie.

Publications (1)

Publication Number Publication Date
WO1993023447A1 true WO1993023447A1 (en) 1993-11-25

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PCT/NL1993/000097 Ceased WO1993023447A1 (en) 1992-05-15 1993-05-12 Binder composition for powder coatings for use as a top coat in the automotive industry and top-coated automotive substrates

Country Status (8)

Country Link
US (1) US5580660A (enExample)
EP (1) EP0640106B1 (enExample)
CN (1) CN1078981A (enExample)
AU (1) AU4358893A (enExample)
BE (1) BE1005819A3 (enExample)
DE (1) DE69309459T2 (enExample)
TW (1) TW270937B (enExample)
WO (1) WO1993023447A1 (enExample)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0703256A1 (en) 1994-09-21 1996-03-27 Dsm N.V. A powder paint binder composition
EP0799844A1 (de) * 1996-03-26 1997-10-08 Hüls Aktiengesellschaft Verfahren zur Herstellung von in der Hitze härtbaren wetterstabilen Polyurethan-Pulverlacken sowie die danach erhaltenen Beschichtungen
EP0816411A1 (de) * 1996-07-04 1998-01-07 Hüls Aktiengesellschaft Blockierte Polyisocyanate, ein Verfahren zu ihrer Herstellung sowie deren Verwendung
EP0822211A1 (de) * 1996-08-02 1998-02-04 Bayer Ag Mit 3,5-Dimethyl-1,2,4-triazol blockierte Polyisocyanate
EP1028135A1 (en) * 1998-12-28 2000-08-16 Bayer Corporation Method for making 1,2,4-Triazole blocked polyisocyanate crosslinkers, coating compositions and coatings prepared therefrom
EP1114101A4 (en) * 1998-09-18 2001-12-12 Mcwhorter Technologies Inc POWDER COATINGS BASED ON BRANCHED OLIGOESTERS AND TRIAZOL-BLOCKED POLYISOZYANATES

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DE19725742C2 (de) * 1997-06-18 1999-11-04 Herberts & Co Gmbh Verwendung von Harnstoffverbindungen und Formaldehyd liefernden Substanzen in Klarlacküberzugsmitteln
US6255523B1 (en) 1998-09-18 2001-07-03 Mcwhorter Technologies, Inc. Power coatings based on branched oligoesters and non-emissive uretdione polyisocyanates
DE10335491A1 (de) * 2003-08-02 2005-02-24 Basf Coatings Ag Thermisch härtender, transparenter Beschichtungsstoff, Verfahren zu seiner Herstellung und seine Verwendung
US7214432B2 (en) * 2003-09-30 2007-05-08 General Electric Company Coating compositions, their preparation, and coated articles made therefrom
JP2007514521A (ja) * 2003-11-03 2007-06-07 エムアイ６ テクノロジーズ，インク． スプレー用塗装保護フィルム及びその適用方法
CN101191029B (zh) * 2006-12-01 2011-05-18 比亚迪股份有限公司 用于金属基材的底层涂料组合物及其制备方法和多层涂层
TWI526506B (zh) * 2010-09-21 2016-03-21 Arakawa Chem Ind Non-aqueous primer with plastic film with reactive energy ray hardening film, plastic film with hardening film with active energy line
US9359524B2 (en) * 2013-10-15 2016-06-07 Ppg Industries Ohio, Inc. Polyesters and coatings containing the same
CN108977039A (zh) * 2018-08-07 2018-12-11 太仓佩琦涂料有限公司 双重固化uv清漆

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3721645A (en) * 1971-02-25 1973-03-20 Liner Technology Inc Polyurethanes stabilized with 1,2,3-,1,2,4-1,2,5-,and 1,3,4-triazoles
EP0004571A1 (de) * 1978-03-21 1979-10-17 Bayer Ag 1,2,4-Triazol-blockiertes Isophorondiisocyanat und Biuretgruppen oder Urethangruppen aufweisende Derivate des Isophorondiisocyanats mit 2 bis 4 1,2,4-triazol-blockierten Isocyanatgruppen und Pulverlackbindemittel, die diese Derivate als Vernetzer enthalten
EP0224165A2 (de) * 1985-11-27 1987-06-03 Bayer Ag Verfahren zur Herstellung von Isocyanuratgruppen aufweisenden Polyisocyanaten und ihre Verwendung als Isocyanatkomponente in Polyurethanlacken
EP0224915A2 (en) * 1985-12-03 1987-06-10 E.I. Du Pont De Nemours And Company Amine vapor curable coating composition of an acrylic polymer and a polyisocyanate
EP0286799A2 (de) * 1987-04-04 1988-10-19 Hüls Aktiengesellschaft Polyurethan-Pulverlacke, die nach Aushärtung eine matte Oberfläche ergeben
US4824909A (en) * 1986-04-10 1989-04-25 Nippon Paint Co., Ltd. Powder coating composition

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BE1008721A3 (nl) * 1994-09-21 1996-07-02 Dsm Nv Bindmiddelsamenstelling voor poederverfformuleringen.
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KR100650830B1 (ko) * 1998-09-18 2006-11-27 이스트만 케미칼 캄파니 분지된 올리고에스테르 및 트리아졸 블록화된폴리이소시아네이트를 기재로한 분말 코우팅
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BE1005819A3 (nl) 1994-02-08
EP0640106B1 (en) 1997-04-02
TW270937B (enExample) 1996-02-21
DE69309459T2 (de) 1997-10-23
EP0640106A1 (en) 1995-03-01
US5580660A (en) 1996-12-03
CN1078981A (zh) 1993-12-01
DE69309459D1 (de) 1997-05-07
AU4358893A (en) 1993-12-13

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