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
  • C08G18/08—Processes
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
  • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
  • B05D5/00—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
  • B05D5/06—Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures to obtain multicolour or other optical effects
  • B05D5/067—Metallic effect
  • B05D5/068—Metallic effect achieved by multilayers
• • 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
  • C08G18/4202—Two or more polyesters of different physical or chemical nature
• • 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
  • C08G18/61—Polysiloxanes
• • 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
  • C09D175/06—Polyurethanes from polyesters

Definitions

• electrically discontinuous metal layers have been developed which appear as continuous metal layers to the naked eye, which are less susceptible to widespread corrosion and which can be applied to flexible substrates.
• These electrically discontinuous layers consist of discrete metallic islands, which are vacuum deposited on the substrate, wherein the islands are separated by channels. These islands and channels are then top coated with a dielectric polymeric coating to separately encapsulate each island and to prevent corrosion of the metal islands.
• the top coat has experienced a loss of adhesion (e.g., peel) from the metal islands and substrate in the channels and water infiltration.
• the metal layer has been etched with a caustic (e.g., sodium hydroxide solution) to remove metal deposited in the channels between the islands to provide a larger substrate surface area for bonding with the top coat .
• a caustic e.g., sodium hydroxide solution
• caustic etching has resulted in the formation of blackened areas in the metal layer.
• This invention relates to a metallized article comprising a substrate having a layer of electrically discrete metallic islands of a corrosion prone metal disposed on the substrate.
• a polyurethane basecoat layer is formed on th substrate prior to forming the metallic islands thereon.
• a crosslinked polyurethane top coat, bound to an organosilane, preferably an epoxy silane, is disposed on and encapsulates the discrete metallic islands.
• the organosilane is also is bound to the metallic islands.
• the advantage of this invention is that it improves the bonding of polyurethane top coat to the basecoat or substrate, and to the metal layer deposited on the substrate, without caustic etching of the metal layer.
• This invention also increases the water resistance (hydrophobicity) of the top coat by increasing polymeric crosslinking within the top coat, thereby enhancing corrosion resistance.
• the substrates of the present invention include any substrate upon which a reflective metallic coating is desirable. These substrates can be rigid or flexible.
• substrates and may or may not be electrically conductive.
• substrates used in the present invention include vehicular/automotive trim applications, sheet stock, sports equipment, clothing and any other items suitable for decoration by inclusion of a reflective metallic sur ace.
• nonconductive (dielectric) substrates include a wide variety of plastic substrates which are dielectric materials (non-conductive) including thermoplastic materials, thermosetting materials and elastomeric materials, such as thermoset polyurethane, flexible elastomers which may be a natural or synthetic thermoplastic or thermoset polymer having an elongation of at least 30%, polyolefins, as polyethylene, polypropylene, polybutylene or a rubber/polypropylene blend, ABS (polyacrylonitrile-butadiene-styrene) , thermoplastics as polyvinyl chloride, Surlyn (DuPont) , polyester, polyester elastomer, and the like.
• plastic substrates which are dielectric materials (non-conductive) including thermoplastic materials, thermosetting materials and elastomeric materials, such as thermoset polyurethane, flexible elastomers which may be a natural or synthetic thermoplastic or thermoset polymer having an elongation of at least 30%, polyolefins,
• Plastic substrates include, for example, automobile parts such as exterior moldings, bumper guards, dual pulls, mirror housings, grill headers, light bezels, gear shift bezels, door pulls, steering wheel emblems and other exterior and interior automotive trim components.
• Other plastic articles can be used, for example in the plumbing trade, for household hardware applications, for home decoration, trucks, motor cycles and marine parts.
• suitable conductive substrates include metals, such as aluminum, aluminum alloy, carbon steel, cast iron, brass, copper, nickel, nickel alloy, stainless steel, magnesium alloy and zinc based materials.
• Articles comprising metal substrates include, for example, faucets, knobs, handles, cutlery, files and blades, golf clubs and irons, hammers, jet blades, rifle barrels, skate blades, camera components and luggage.
• the metal substrate is a vehicle wheel.
• these substrates may be pretreated prior to the present application process.
• Such pretreatment may optionally include pickling and/or the application of corrosion resistant coatings.
• Those corrosion resistant coatings can be phosphate corrosion resistant coatings or epoxy primers such as "E-coat", i.e., a cathodic electrocoat or a coating utilizing powder particles.
• E-coat i.e., a cathodic electrocoat or a coating utilizing powder particles.
• a corrosion resistant coating may include well known chromium conversion coatings and the like.
• an adhesion promoter may be applied to non-metallic substrates, such as chlorinated polyolefin to thermoplastic olefins. Typically, a coating thickness of about 0.1 mils to about 0.4 mils is applied.
• the preferred substrates for the present invention are flexible substrates.
• the metals that are used to form the layer of metallic islands are metals, or surface oxidized metals that will give a bright surface. Suitable metals are corrosion prone metals including tantalum, copper, silver, nickel, chromium, tin and aluminum and alloys thereof, and the like. Preferably, the metallic islands contain indium, indium alloys and/or indium oxides .
• the layer of metallic islands is formed by depositing metal on the substrate, or coated substrate, by thermal evaporization, sputtering, ion plating, induction heating, electron beam evaporization and like methods. More uniform coverage is obtained, particularly around corners, edges or recesses if the metallization occurs in a chamber containing an inert gas such as argon.
• Metallization produces a substrate that has a layer of discrete metallic islands deposited thereon.
• the discrete metallic islands are round in nature and have a thickness, or diameter, small enough to make the metallic film electrically non-conductive, as there are channels between the islands such that there is typically no conductivity between the islands, and alternately large enough to reflect enough light to make the coated article appear as a metal article to the naked eye.
• the thickness of the metallic islands will be between about 25 and about 4000 Angstroms (A) , preferably 500- 3000A. Most preferably, the thickness is between about 500A- 1200A.
• the layer of metallic islands on the substrate is encapsulated by a top coat.
• a prime coat and/or basecoat was also applied to the substrate prior to metallization.
• the coating composition for the prime coat, basecoat and/or top coat, after curing is a polyurethane or a polyester polyurethane.
• a resin suitable for forming basecoats and top coats useful in the present invention is described in Example 1.
• At least one organosilane is added to the top coat resin.
• organosilanes A description of the use of organosilanes in resin top coats, for application to metal island layers, is described in U.S. Patent Application Serial No. 08/576,072, files August 25, 1996, which is incorporated in its entirety herein by reference .
• At least one organosilane must be an organosilane that will react with the polyurethane and with the metal islands, preferably an epoxy silane, and more preferably gamma- glycidoxypropyltrimethoxy silane .
• An epoxy silane which as an additive in the top coat composition, co-reacts upon heating with the urethane resin during curing. While the Applicants do not wish to be bound to any particular theory, it is believed that the epoxide ring of the epoxy silane generally reacts with the isocyanate groups of the urethane resin. It is also believed that a portion of the silane group SiR 1 R 2 R 3 , wherein R X ⁇ R 2 ( R 3 can be hydroxyl or alkoxy, in one or more steps reacts to bond to the metal of the islands (or metal hydroxides coating the surface of the metal islands) . Alternately, it is to be understood that the epoxy silane may be reacted with the urethane portion of the coating material prior to the application of the coating.
• the prime coat or basecoat may also be crosslinked to the top coat and/or bound to the metallic islands from epoxy silane contained in the top coat of from epoxy silane that was previously added to the prime coat or basecoat.
• the amount of epoxy silane used in the coating is an amount sufficient to bond the polymeric top coat to the metallic islands without clouding the top coat.
• the weight of epoxy silane is between about 0.25% to about 8.0%.
• An example of a suitable top coat containing an epoxy silane is described in Example 3.
• the topcoat contains both an epoxy silane, such as gamma-glycidoxypropyltrimethoxy silane and a secondary aminosilane, such as bis- (gamma- trimethoxysilylpropyl) amine, to further harden the coat(s) by increasing the degree of polymeric crossliking within the coat.
• an epoxy silane such as gamma-glycidoxypropyltrimethoxy silane
• a secondary aminosilane such as bis- (gamma- trimethoxysilylpropyl) amine
• the coating compositions whether they be base coat and/or top coat is cured at a temperature that is high enough to completely cure the coating material but low enough such that the coating does not burn or significantly discolor.
• the coating is cured at a temperature range of approximately 150-375°F, for a period of time of about 10 minutes to about 70 minutes, and with controlled humidity, typically with a dew point between about 96°F to about 105°F.
• the coating is preferably cured at a temperature between about 250°F to about 300°F.
• the thickness of the coating is typically between about 1 mil to about 5 mils. Preferably, the coating thickness is between about 1.5 mils to about 2.5 mils.
• a coating is applied in an organic solvent system wherein the organic solvent (s) comprise about 40% to about 90% of the weight of the pre-cured coating composition.
• the urethane resin is typically about 10% to about 50% by weight of the pre-cured coating composition.
• organic solvents can be utilized for the commercially available coating compositions, such_ as aromatic hydrocarbons, alkylesters, alcohols, ketones and dialkylethers " .-
• the organic solvent is a solvent blend as is described in Examples 2 and 3.
• the application of the coating system described herein is preferably performed by an airless spray gun.
• the coatings are applied to the substrate at ambient temperature and pressure .
• inorganic carriers such as carbon dioxide
• the method for applying a coating with a reduced amount of organic solvent is described in U.S. Patent Number 5,464,661 which is incorporated herein by reference.
• the Unicarb® System (Union Carbide) is a useful apparatus for replacing liquid organic solvent with C0 2 in spraying coatings in the present invention.
• the coatings are typically flashed for approximately 10 to 20 minutes to evaporate the solvents in the coating system and optionally by a curing step after application of each layer.
• the substrate is in a handleable or tacky condition, prior to application of metal.
• additional amounts of pigment may be added for a prime or a basecoat typically in the amount of about 0.1% to about 40% by weight of the pre-cured (e.g. sprayable) coating composition, Preferably, the amount of pigment is between about 2% to about 30% by weight.
• Catalysts to promote the reaction between the silaceous containing material and the coating composition may be such materials as tin containing or amine containing such as di-n- butyltin dilaurate, tri-ethylenediamine and the like.
• the amount of catalyst in the pre-cured coating composition is between about 0.1% to about 10% by weight .
• Capralactone triol 491.3 lbs. of Stock No. PO305 from Union Carbide
• hydroxy terminated polysiloxane copoly ⁇ ner 14.7 lbs. of DC193 from Dow Corning
• Blend Component I After drying for an hour, the nitrogen purge of the reactor was restarted. Then, 253 lbs. of urethane grade toluene were added to the reactor over a 3-5 minute interval. After raising the reactor temperature to 220°F over a ten minute interval, an additional 253 lbs. of toluene were added over a 3-5 minute interval to form Blend Component I.
• Hexanediol adipate (240.2 lbs. of Fomrez 66-112 from Witco Chemical) was added to a second reactor, nitrogen blanketed and heated to 150°F under agitation, the nitrogen blanket was then secured and the hexanediol adipate was dried under vacuum. After drying for an hour, the nitrogen purge was restarted. Over a 3-5 minute interval, 240.2 lbs. of toluene were added to the reactor, while maintaining the temperature at 150°F, to form Blend Component II.
• Blend Component I The urethane blend was then formed from Blend Component I and Blend Component II. Initially, 753.36 lbs. of hydrogenated methylene diisocyanate (Desmodur W from Bayer) were added to a reactor. While stirring, and with nitrogen blanketing, 0.14 lbs. of dibutyl-10-dilaurate (Dabco 12 from Air Products) were added to the reactor. The nitrogen blanketing was then secured. After the reaction temperature reached 100°F, the reactor was cooled by injecting cold air into the reactor. Then, over a forty minute interval, 1012 lbs. of Blend Component I were added to the reactor. During a subsequent forty minute interval, 600 lbs. of toluene were added to the reactor.
• Reactor cooling was secured and then the reactor was maintained at 100°F, with stirring, over a subsequent hour long interval.
• Blend Component II (480.4 lbs.) was added to the reactor over a 5-10 minute interval while maintaining reactor temperature at about 150°F. Then 153.4 lbs. of toluene were added to the reactor over a 3-5 minute interval after which the reactor was maintained at 150 ⁇ 20°F for an hour.
• Example 2 Synthesis of a Basecoat Composition
• the basecoat resin to be applied to the substrate was formed by mixing 39.9 grams of a urethane blend with 1.6 grams of the tin catalyst (5% UL-28, Witco Chemicals, containing 5% solids), 23.4 grams of a polyester resin containing carbon- black (3090 Tint paste, purchased from PPG, containing 40% solids) and 35.1 grams of a solvent blend.
• the urethane blend was similar to that in Example 1 with the exception that the resin is in toluene instead of xylene and contains 40% solids instead of 50% solids.
• the solvent blend used contains 60 wt. % propylene glycol methyl ether acetate (PMA) , 25 wt. % dispropylene glycol methyl ether acetate (DPMA) , and 15 wt. % of a blend of dibasic esters (purchased from Dupont) containing 55-65% dimethyl glutarate, 10-25% dimethyl adipate and 15-25% dimethyl succinate (hereinafter "DBE" ) .
• PMA propylene glycol methyl ether acetate
• DPMA dispropylene glycol methyl ether acetate
• DBE dibasic esters
• the metal-bonding top coat of the present invention was synthesized by mixing the urethane blend of Example 1 with the silane additive gamma-glycidoxypropyltrimethoxy silane (A187 purchased from OSi Specialties, Danbury, Connecticut) .
• a solvent blend (5345 grams) was added to a reactor using an automated delivery system.
• the solvent blend contains 62.5 wt . % propylene glycol methyl ether acetate (PMA), 22.5 wt . % xylene, 10 wt. % dipropylene glycol methyl ether acetate (DPMA) and 5 wt . % DBE.
• the top coat resin was maintained under agitation until application.
• the delta color reading "b*" for the etch top coat- was about 7.5, 27 and 29 at 10, 15 and 20 cycles, respectively.
• the delta color reading w b*" for the non-etch top coat was about 6.5, 18.5 and 31 at 10, 15 and 20 cycles, respectively.
• the delta color reading "a*” for the etch top coat was about 1, 2 and 15.5 at 10, 15 and 20 cycles, respectively.
• the delta color reading "a*” for the non-etch top coat was about 1, 1 and 6 at 10, 15 and 20 cycles, respectively.
• the delta color reading "Y" for the etch top coat was about 14, 19 and 23 at 10, 15 and 20 cycles, respectively.
• the delta color reading "Y” for the non-etch top coat was about 4, 16 and 18 at 10, 15 and 20 cycles, respectively.
• the delta color reading "X" for the etch top coat was about 8, 11.5 and 14 at 10, 15 and 20 cycles, respectively.
• the delta color reading "X" for the non-etch top coat was about 2, 8 and 10 at 10, 15 and 20 cycles, respectively.

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• Organic Chemistry (AREA)
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• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Laminated Bodies (AREA)
• Application Of Or Painting With Fluid Materials (AREA)
• Paints Or Removers (AREA)

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• 1997
  • 1997-03-01 EP EP97908775A patent/EP0979151B1/de not_active Expired - Lifetime
  • 1997-03-01 WO PCT/US1997/003155 patent/WO1998037985A1/en active IP Right Grant
  • 1997-03-01 WO PCT/US1997/003333 patent/WO1998037986A1/en not_active Application Discontinuation
  • 1997-03-01 EP EP97908841A patent/EP0963258A1/de not_active Withdrawn

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