GB1573008A - Metallized flexible plastics automobile trimcomponent - Google Patents

Metallized flexible plastics automobile trimcomponent Download PDF

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Publication number
GB1573008A
GB1573008A GB51904/76A GB5190476A GB1573008A GB 1573008 A GB1573008 A GB 1573008A GB 51904/76 A GB51904/76 A GB 51904/76A GB 5190476 A GB5190476 A GB 5190476A GB 1573008 A GB1573008 A GB 1573008A
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article
pass
coat
acrylic
baked
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McCord Corp
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McCord Corp
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00Layered products comprising a layer of synthetic resin
    • B32B27/06Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/042Coating with two or more layers, where at least one layer of a composition contains a polymer binder
    • C08J7/0423Coating with two or more layers, where at least one layer of a composition contains a polymer binder with at least one layer of inorganic material and at least one layer of a composition containing a polymer binder
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/043Improving the adhesiveness of the coatings per se, e.g. forming primers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/046Forming abrasion-resistant coatings; Forming surface-hardening coatings
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • C23C14/20Metallic material, boron or silicon on organic substrates

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Polymers & Plastics (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Laminated Bodies (AREA)
  • Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)

Description

(54) METALLIZED FLEXIBLE PLASTICS AUTOMOBILE TRIM COMPONENT (71) We, McCORD CORPORATION, of 2850 West Grand Boulevard, Detroit, Michigan 48202, United States of America, a corporation organised and existing under the laws of the State of Michigan, United States of America, do hereby declare the invention for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in the following statement: The present invention relates to a metallised plastics article having a composite coating which is built up in a specific manner from certain selected films or ingredients.
Vacuum metallizing of plastics surfaces has been practiced for some time. For example, see U. S. Patents Nos. 3,201,271; 3,740,254; 2,993,806; and 3,783,012. More recently, attempts have been made to manufacture automobile exterior trim components such as bumpers, bumper sections or fender extensions of a tough but flexible, abuse-resistant plastics material having a bright metal-like surface. Generally speaking, such metallized sufaces have not had the low-temperature flexibility, the resistance against impact from gravel, the corrosion resistance, and the chrome-plated appearance, required for automotive use. An article in the December 1974 issue of Modern Plastics, "Restoring the Lustre to Metallized Markets", pp.42-46, by C. Otis Post presents a good summary. In that article it is noted with regard to making metallized coatings environmentally acceptable that: "The relationships among a plastics substrate, base coat, metallized coating, and top coat are so intricate that changing any one member usually means reformulating one or more of the others." According to one aspect of the invention there is provided a metallized plastics article comprising: a flexible elastomeric plastics substrate, the surface of which tends to degrade upon exposure to light, a light-blocking continuous pigmented polymeric layer thereon, the pigment content and thickness thereof being sufficient to ensure that any amount of light detrimental to said plastics-substrate does not pass therethrough, a deposited metal film overlying the polymeric layer less than 1000 thick, and a continuous non-opaque protective polymeric top coat over said metal film.
According to another aspect of the invention there is provided a metallized plastics article comprising: a) a flexible elastomeric plastics substrate b) a light-blocking pigmented primer coat on a surface of said substrate, c) a base coat over said primer coat of a baked thermosetting resin, d) a vacuum deposited layer thereon of a metal selected from the group consisting of chromium, stainless steel and aluminum, said layer being in the range of 200 to 1000 thick, and e) a moisture impervious flexible film thereover of a non-opaque acrylic lacquer.
According to a further aspect of the invention there is provided a metallized plastics article which includes a synthetic polymeric substrate that tends to degrade upon exposure to sunlight, a light blocking pigmented polymeric layer thereon, a deposited metal film overlying the polymeric layer and a transparent protective polymeric topcoat over said metal film, said metal film being minutely fissured permitting passage of light, and the pigment content and thickness of said pigmented polymeric layer being sufficient to stop passage of said sunlight from said fissures.
And according to a further aspect of the invention there is provided a metallised plastics article comprising (a) a flexible elastomeric plastics substrate, (b) a pigmented primer coat on a surface of said substrate, (c) a clear base coat over said primer coat of a baked blend of an aliphatic urethane resin with an anhydride cured epoxy resin, (d) a vacuum deposited layer thereon of a metal, and (e) a clear abuse resistant film thereover of a baked blend of acrylic, aliphatic urethane and melamine resins.
The metallizing may involve the use of vacuum deposited chromium or stainless steel such as a "ferrous-chrome" containing 13% to 30% chromium when the part is designed for exterior use on an automobile. Such a stainless steel or chromium coated part can also be used in the interior of an automobile such as for trim for an instrument cluster. One may prefer to use aluminum instead of stainless steel where weathering and abuse resistance are not too important as aluminum gives a more pleasing chromium plated-like appearance, i.e. it more nearly duplicates the appearance of conventional electroplated chrome parts. However, when a thin layer of aluminum oxidizes it becomes transparent or translucent and the metallic luster is lost. In an exterior application such as a bumper section, if there is a break or blemish caused by a stone nick or the like, an aluminum layer disappears at the break or blemish point in a short period of time and then will continue to oxidize and disappear until the entire aluminum layer is gone.
The base plastics material from which the part is made is a tough but flexible elastomer, preferably an injection molding grade thermoplastic polyurethane (TPU). By "flexible elastomer" is meant a natural or synthetic thermoplastic or thermoset plastics material or polymer having an extensibility of greater than approximately 30 percent, as compared to a "rigid" plastics material which may be considered to have an extensibility of less than 10 percent. While it is preferred to use a molded thermoplastic urethane because of its other properties, such a urethane is more deleteriously affected by sunlight than many other plastics, that is, it is light sensitive.
An article of the desired shape made from the elastomer, after surface cleaning if required, may be successively coated in accordance with the present invention with preferably four well-bonded layers or films to produce the final lustrous metallic appearance desired.
The cleaned plastics part is first prime coated with a pigmented and thus light-blocking urethane lacquer having a dry film thickness of 0.8 to 1.2 mils, which is air flashed and baked.
While aromatic urethanes have been used, the urethane is preferably an aliphatic one which is inherently more light stable. This is followed by a base coat of a melamine formaldehyde resin or preferably, a urethane-epoxy resin having a dry film thickness of about 0.8 to 1.2 mils. The base coat is also baked, and if it were applied directly to the plastic substrate, it would not adhere well. On the other hand, the pigmented urethane lacquer prime coat will not flow readily and form the level, sheeny and smooth uniform surface required for the vacuum deposited metal. Desirably, the base coat should also be light stable.
Depending on the appearance desired in the final part, the base coat can be applied to be sheeny or to be matte appearing. It is preferred to apply the base coat "wet-on-wet" directly onto the air-flashed but not completely baked primer as better intercoat adhesion is obtained.
The base coat when dry may be glossy so that the finished article has a sheeny metallic appearance. is then The metal is then vacuum deposited onto the base coat using preferably the resistance method. Electron beam and sputtering vacuum depositing can also be used. Sputtering gives a deposit that is brighter appearing than the others, but a lacquer top coating thereover tends to microcrack in the metal layer. Resistance coating is favored as the required investment in equipment is substantially less.
The metal coating is preferably 200-1000 A thick -- thick enough to develop the proper metallic color. If stainless steel is used, its chromium content is essential, but the steel can also have incorporated therein minor amounts of nickel and/or magnesium and/or other metals.
The use of essentially pure chromium is included within the ambit of this invention because, contrary to what some believed, it was found that chromium could be successfully vacuum deposited for this application. Essentially pure aluminum gives the more pleasing appearance and most closely matches that of traditional electrodeposited chromium on metal parts.
Chromium deposited by resistance vacuum metallizing is the next most effective in matching qlectrodeposited chromium.
The thin metal coating is not, of course, resistant to mechanical abuse and to long term weathering and needs to be protected. While various flexible abuse-resistant non-opaque top lets, such as an acrylic lacquer might be used, it has been found that a clear lacquer derived from a blend of acrylic, aliphatic urethane and melamine resin has definite advantages and is tobe preferred. This particular top coat can also be used in other applications such as for the protection of painted parts.
The film thickness of the top coat is preferably in the range of 1.3 to 1.6 mils, dry basis, and it is preferably thoroughly baked, e.g. at 2500F, but too high a temperature may cause some yellowing and/or iridescence. The top coat is formulated to adhere to the metal layer as well as to the base plastics material. By deliberately overlapping the top coat, the metal coat and the two underlying layers can be "encapsulated" between it and the base plastics material eliminating edge delamination.
The development work on this invention turned up an interesting finding, viz: that light may penetrate the metal coating and base coat film and reach the surface of the underlying primer coat, causing degradation thereof and interfacial loss of adhesion between the base coat and the primer coat. That light penetrates the metal film, which appears to the eye to be continuous and opaque, is surprising. This was found to be so as follows: When a metallized layer deposited on a film of the base coat supported on a glass plate is exposed to visible light, including ultraviolet light rays, the light will not pass through. When, however, the acrylic top coat is applied thereover and baked, some of the light will pass through. It is belived that this is because minute, microscopic cracks or fissures through the metal film were formed which allowed the light to pass. Apparently the solvents normally used in the top coat material and the difference in thermal expansion of the metal and resin films during baking cause these minute cracks to appear.
As the light does pass through the metal layer, as the base coat is not pigmented, and as the thermoplastic urethane base part is quite light sensitive, the skilled in the art will appreciate that it is quite desirable to make the primer coat light opaque and to use a resin therein that is, preferably, inherently light stable, such as an aliphatic urethane. Long term outdoor, e.g.
Florida sunshine for one year, weathering tests have conclusively established that interfacial adhesion loss will occur between the base coat and the primer coat before it will occur at the interfaces of the other layers. Use of a properly formulated, pigmented and applied primer coat will offset this interfacial adhesion loss.
There is little question that this finding of light penetration and effect is an important one that lends considerable merit to the present claim for inventiveness for the described multi-layered metallized product. And, of course, as the metal film is in a sense deliberately micro-crazed or minutely cracked in a controlled regulated manner, this permits later flexing and bending of the product without appreciable or too objectionable change in its appearance. Moreover, light is reflected back through these microscopic cracks to some extent, and this characteristic can be used to esthetic advantage. A white or tinted light-blocking pigmented primer coat can be effectively employed to advantageously change the appearance of the metal layer and enhance the overall appearance of the multi-layered metallized plastics article.
THE DRAWING The drawing is a greatly enlarged schematic cross-sectional view of a metallized surface made according to this invention, in which the number designating the layers are: 1) Injection molded thermoplastic urethane.
2) Baked urethane lacquer.
3) Baked melamine formaldehyde resin.
4) 800 A vacuum deposited ferrous-chrome-20 stainless steel.
5) Clear acrylic lacquer.
EXAMPLE I The sample part made was a 1975 Cadillac (Registered Trade Mark) Fender Extension, part number X1605647.
An elastomeric thermoplastic urethane was "in house" manufactured from a grafted poly (oxypropylene) diol (Union Carbide Company's NIAX D-432, (Niax is a Registered Trade Mark) 270 Park Avenue, New York, New York 10017), 100 parts by weight; polytetramethylene ether glycol (Quaker Oats Company Polymeg 100, Merchandise Mark Plaza, Chicago, Illinois 60654), 28 parts; 4" 4' diphenylmethane diisocyanate, 86 parts; and 1, 4 butanediol, 26 parts. This thermoplastic urethane is fully described in U.S. Patent No.
3,933,938. Commercially available Uniroyal thermoplastic urethane designated E-2A could also be used (Uniroyal, Inc., 1230 Avenue of the Americas, New York, New York 10020).
The nature of the flexible urethane substrate does not appreciably affect the performance of the applied coating. The urethane cannot be so stiff or rigid that it will not serve its intended function as a flexible trim component nor can it be too flexible or elastomeric. The present coating system can, of course, be applied and used with a substantially more rigid substrate, but other methods of bright trimming such as plating may be more economical to use on firm or hard surfaces.
The urethane lacquer primer was a standard production item supplied by PPG Industries, 3800 West 143rd Street, Cleveland, Ohio, under the code designation DEL-600-32906. Any equivalent light-blocking primer that adheres well to the molded thermoplastic urethane can be used. The one used was a thermoplastic and was not considered too stable to ultraviolet light as it was an aromatic urethane. It was pigmented to a gray color with black and white pigments. The primer was sprayed as supplied by the manufacturer in three or four passes onto the properly cleaned surface at room temperature to a thickness of 1.0 + 0.2 mils (dry basis).
The applied coating requires an air flash for 10 minutes or so, but it was not baked at this point. One of the findings made during the development of this invention was that the subsequent base coat could be applied "wet-on-wet" with improved intercoat adhesion and the consequent saving coming from the elimination of the primer baking step.
The base coat applied over the primer also was a commercially available tough melamine formaldehyde resin, diluted to spray viscosity of 38 + 2 seconds (No. 1 Zahn Cup). The base coat was SM-1240-6, supplied by Red Spot Paint & Varnish Co., Inc., 100 Main Street, Evansville, Indiana. It was applied to a thickness of 1.0 + 0.2 mils. The coating was air flashed for 15 minutes, and then the two coatings were baked for 45 minutes at 2500F + 5 F (oven air temperature).
After cooling to room temperature, the parts were vacuum metallized using an Airco Temescal (Registered Trade Mark) electron beam metallizer. The metal used was a ferrouschrome-20 stainless steel supplied by Airco Temescal, 2850 Seventh Street, Berkeley, California 94710, and it was applied to a thickness of 800 A + 200 . The procedure used was as follows: 1) Metallizer was brought up to and maintained at steady state condition as per manufacturer's instructions.
2) Samples were loaded into the interlock chamber.
3) Chamber was sealed and brought down to proper vacuum.
4) Samples were moved into the metallizing chamber, through the metal vapor cloud and back to the interlock chamber.
5) Interlock chamber was pressurized and the samples were removed.
The top coat was a solvent based acrylic lacquer spray applied by conventional methods.
The base material is supplied by Pan Chemical Corp., 1 Washington Avenue, Hawthorne, New Jersey, as 68-1 89A or 68-202A. The coating was applied to a thickness of 1,3 to 1.6 mils (dry basis) followed by air flashing for 15 minutes and baking at 1500F + 2"F (oven air temperature) for 60 minutes.
Thermoplastic urethane (TPU) Cadillac Fender Extensions made with the "in house" material and metallized and coated as above described were subjected to various tests with the results as given in the following Table.
TEST RESULTS Test Results 200 Weatherometer Hours (3) Slight dulling and water spotting Water Immersion (3) Pass Tape Adhesion (3) Pass Thermal Cycle Pass C.A.S.S. Test (1) Pass Cold Flex (3) Substrate Pass Finish Cracked Gravelometer (SAE Test J-400) Pass Salt Spray (2) Pass Gravelometer plus C.A.S.S. (3) Pass Gravelometer plus Salt Spray (3) Pass Car Wash (3) at 1/2So Pass at5% Pass (1) General Motors Test 4476-P (2) General Motors Test 4298-P (3) According to Cadillac Bright Trim Specifications EXAMPLE II The coating of Example I is applied to an instrument gauge rim with the only difference be ng that an aluminum is used in place of the stainless steel. The aluminum is a 99.99 No high pfflRy aluminum supplied by R. H. Cheney Inc. of Attleboro, Massachusetts 02703, and is appBed to a thickness of 800 A + 200 A. This part is suitable for use in the interior of an automobile.
For critical exterior use, PPG Industries Durethane 300 is preferably used as the primer.
This is a pigmented enamel instead of a lacquer and is based on a thermosetting resin. The resin is an aliphatic urethane which is more light stable than the aromatic urethane of the DEL-600-32906. Durethane 300 is weatherable, flexible at low temperatures and possesses good adhesion affinity for the molded thermoplastic urethane surface.
Durethane 300 is white in color and it has been found that this underlying white coat material enhaces the pleasing metallic appearance of the product, i.e. the metal film is usually thin enough such that the color of the primer coat can be seen through the metal film.
Obviously, in some instances it may be desirable to tint the primer coat to improve the appearance of the part. Also, the use of a white primer coat has the additional advantage that if the metalfilm is scratched or scored, the white shows through, i.e. one sees the white which is complimentary to the metal and not some disfiguring color such as black or gray.
The following formulation has been found to work exceptionally well as a base coat tormulation in place of the previously described Red Coat SM-1240-6.
Parts by weight 50.0 Aliphatic urethane #1 (40%solids) 50.0 Epoxy resin (1) 3.0 HHPA (2) 3.0 Catalyst solution (3) 4.0 Cellosolve acetate (4) 46.0 Methyl-ethyl ketone 50.0 156.0 1 3, 4 epoxy cyclohexylmethyl -3,4 epoxy cyclohexane carboxylate 2 hexahydrophthalic anhydride 3 five parts by weight uranyl nitrate, balance Cellosolve acetate 4 Union Carbide trade name for 2, ethyloxyethyl acetate.
Cellosolve is a Registered Trade Mark.
The aliphatic urethane solution #1 was based on reacting epsilon caprolactone polyester diols and triols with cyclohexyl diisocyanate (CHDI) at 50% solids in toluene, followed by dilution to the 40% solids level with additional toluene. The polyesters were Union Carbide Corporation's NIAX PCP-0200 (the diol) and NIAX PCP-0300 (the triol) and were reacted as follows: Parts by weight PCP-0300 14.698 PCP-0200 3.498 CHDI (1) 21.799 Toluene 59.994 Catalyst (2) 0.011 100.000 (1) Hylene W--E.I. duPont de Nemours & Co., 1007 Market Street, Wilmington, Delaware 19808.
(2) Dibutyl tin dilurate Hylene is a Registered Trade Mark.
As can be seen, this base coat formulation is composed of an aliphatic amine blended with an anhydride cured epoxy, with the curing being catalyzed by the uranyl nitrate. This blend was formulated to optimumize flexibility versus hardness and to provide the excellent metal adhesion that the epoxies are noted for. eight ratio of urethane resin to cured epoxy resin in the above is preferably about 3 to 1 but this can vary from 1 to 1 to 1 to 2.
The following formulation has been found to work better as a top coat formulation than the previously described Pan Chemical's 68-202A: Parts by weight Aliphatic urethane #2(40% solids) 30.0 Acrylic (1) 16.0 Melamine (2) 3.0 Catalyst (3) 0.3 Methyl-ethyl ketone 50.0 Cellosolve acetate (4) 60.0 Toluene acetate 40.0 Toluene 199.3 (1) Cyanamid XC-401 1 (Carboxyl functional acrylic)--American Cyanamid Co., South Cherry Street, Wallingford, Connecticut 06492 2 Cyanamid 303 (hexamethoxymethyl melamine) 3 Cyanamid 4040 (acid catalyst) Union Carbide trade name for 2, ethyloxyethyl acetate.
The aliphatic urethane solution #2 was based on reacting epsilon caprolactone polyester triol (NIAX PCP-0300) and 1,6 hexane adipate diol with cyclohexyl diisocyanate (CHDI) at 40% solids level as follows: Parts by weight CHDI (1) 20.092 Catalyst (2) 0.011 PCP-0300 13.495 1, 6 Hexane adipate diol (3) 6.407 Toluene 59.995 100.000 (1) Hylene W 2 Dibutyl tin dilaurate 3 Ageflex 6-1000-Witco Chemical Co., 277 Park Avenue, New York, New York 10017 The weight ratios of the resins in this top coat are such that the aliphatic urethane and acrylic resins are used in about equal amounts, although up to 5 times as much urethane as acrylic can be used. The melamine will usually amount to 5 to 20 weight percent of the acrylic resins.
TPU Cadillac fender extensions made with this metallized bright trim system give the following test results: TEST RESULTS Test Results 500 Weatherometer Hours (3) Slight dulling and water spotting Water Immersion Pass Tape Adhesion (3) Pass Thermal Cycle Pass C.A.S.S. Test (1) Pass Cold Flex (3) Substrate Pass Finish Pass Gravelometer (SAE Test J-400) Pass Salt Spray (2) Pass Gravelometer plus C.A.S.S. (3) Pass Gravelometer plus Salt Spray (3) Pass Car Wash (3) at 1/2% Pass at5% Pass 1 General Motors Test 4476-P 23 General Motors Test 4298-P According to Cadillac Bright Trim Specifications AT WE CLAIM IS: L A metallized plastics article comprising: lexible elastomeric plastics substrate, the surface of which tends to degrade upon expos me to light, a light-blocking continuous pigmented polymeric layer thereon, the pigment .fFx < er x,
**WARNING** end of DESC field may overlap start of CLMS **.

Claims (16)

  1. **WARNING** start of CLMS field may overlap end of DESC **.
    Parts by weight Aliphatic urethane #2(40% solids) 30.0 Acrylic (1) 16.0 Melamine (2) 3.0 Catalyst (3) 0.3 Methyl-ethyl ketone 50.0 Cellosolve acetate (4) 60.0 Toluene acetate 40.0 Toluene
    199.3 (1) Cyanamid XC-401 1 (Carboxyl functional acrylic)--American Cyanamid Co., South Cherry Street, Wallingford, Connecticut 06492 2 Cyanamid 303 (hexamethoxymethyl melamine) 3 Cyanamid 4040 (acid catalyst) Union Carbide trade name for 2, ethyloxyethyl acetate.
    The aliphatic urethane solution &num;2 was based on reacting epsilon caprolactone polyester triol (NIAX PCP-0300) and 1,6 hexane adipate diol with cyclohexyl diisocyanate (CHDI) at 40% solids level as follows: Parts by weight CHDI (1) 20.092 Catalyst (2) 0.011 PCP-0300 13.495 1, 6 Hexane adipate diol (3) 6.407 Toluene 59.995
    100.000 (1) Hylene W 2 Dibutyl tin dilaurate 3 Ageflex 6-1000-Witco Chemical Co., 277 Park Avenue, New York, New York 10017 The weight ratios of the resins in this top coat are such that the aliphatic urethane and acrylic resins are used in about equal amounts, although up to 5 times as much urethane as acrylic can be used. The melamine will usually amount to 5 to 20 weight percent of the acrylic resins.
    TPU Cadillac fender extensions made with this metallized bright trim system give the following test results: TEST RESULTS Test Results 500 Weatherometer Hours (3) Slight dulling and water spotting Water Immersion Pass Tape Adhesion (3) Pass Thermal Cycle Pass C.A.S.S. Test (1) Pass Cold Flex (3) Substrate Pass Finish Pass Gravelometer (SAE Test J-400) Pass Salt Spray (2) Pass Gravelometer plus C.A.S.S. (3) Pass Gravelometer plus Salt Spray (3) Pass Car Wash (3) at 1/2% Pass at5% Pass 1 General Motors Test 4476-P 23 General Motors Test 4298-P According to Cadillac Bright Trim Specifications AT WE CLAIM IS: L A metallized plastics article comprising: älexible elastomeric plastics substrate, the surface of which tends to degrade upon expos me to light, a light-blocking continuous pigmented polymeric layer thereon, the pigment .fFx < er x,
    content and thickness thereof being sufficient to ensure that any amount of light detrimental to said plastics substrate does not pass therethrough, deposited metal film overlying the polymeric layer less than 1000 thick, and a continuous non-opaque protective polymeric top coat over said metal film.
  2. 2. The article of claim 1 wherein said pigment is light coloured.
  3. 3. The article of claim 1 wherein said continuous pigmented polymeric layer is immediately contiguous to said plastics substrate as a primer coat and has had applied directly thereto a base coat of a stable thermosetting resin on to which has been directly applied said metal film by vacuum deposition.
  4. 4. The article of claim 3 in which said article is an exterior automobile trim component, said metal film is formed from a metal selected from the group consisting of stainless steel and chromium, said primer coat is a pigmented urethane lacquer having a dry film thickness of 0.8 to 1.2 mils, said base coat is baked melamine formaldehyde resin having a dry film thickness of 0.8 to 1.2 mils, and said top coat is a baked acrylic lacquer having a dry film thickness of 1.3 to 1.6 mils.
  5. 5. The article of claim 3 when said article is an interior automobile trim component, said metal film is of aluminum, said primer coat is a pigmented urethane lacquer having a dry film thickness of 0.8 to 1.2 mils, said base coat is a baked melamine formaldehyde resin having a dry film thickness of 0.8 to 1.2 mils, and said top coat is baked acrylic lacquer having a dry film thickness of 1.3 to 1.6 mils.
  6. 6. A metallized plastics article comprising: a) a flexible elastomeric plastics substrate, b) a light-blocking pigmented primer coat on a surface of said substrate, c) a base coat over said primer coat of a baked thermosetting resin, d) a vacuum deposited layer thereon of a metal selected from the group consisting of chromium, stainless steel and aluminum, said layer being in the range of 200 to 1000 A thick, and e) a moisture impervious flexible film thereover of a non-opaque acrylic lacquer.
  7. 7. The metallized plastics article of claim 6 wherein said primer coat and said base coat have the characteristics of having been spray-applied wet-on-wet and baked together and wherein said flexible film of said acrylic lacquer extends over the edges of said vacuum deposited layer, base coat, and primer coat onto said substrate, thereby encapsulating the three intermediate coats.
  8. 8. The metallized plastic article of claim 7 when an automobile trim component and wherein said plastics substrate is a molded thermoplastic urethane.
  9. 9. The automobile trim component of claim 8 wherein said base coat, when dry, is glossy such that the finished article has a sheeny metallic appearance.
  10. 10. A metallized plastics article which includes a synthetic polymeric substrate that tends to degrade upon exposire to sunlight, a light-blocking pigmented polymeric layer therein, a deposited metal film overlying the polymeric layer and a transparent protective polymeric topcoat over said metal film, said metal film being minutely fissured permitting passage of light, and the pigment content and thickness of said pigmented polymeric layer being sufficient to stop passage of said sunlight from said fissures.
  11. 11. The article of claim 10 wherein said pigment content imparts a light color to said polymeric layer and said metal film is thin enough to permit the presence of said light color to be visually apparent, as compared with the absence thereof.
  12. 12. The article of claim 10, in which said topcoat comprises a blend of acrylic, aliphatic urethane and melamine resins which have been laid down as a lacquer and then dried and baked.
  13. 13. The article of claim 12 when an automobile exterior trim component and wherein in said blend the weight ratio of said aliphatic urethane resin to said acrylic resin is in the range of 1/1 to 5/1 and said melamine resin is in the range of 5%to 20%by weight of acrylic resin.
  14. 14. A metallised plastics article comprising (a) a flexible elastomeric plastics substrate, (b) a pigmented primer coat on a surface of said substrate, (c) a clear base coat over said primer coat of a baked blend of an aliphatic urethane resin with an anhydride cured epoxy resin, (d) a vacuum deposited layer thereon of a metal, and (e) a clear abuse resistant film thereover of a baked blend of acrylic, aliphatic urethane and melamine resins.
  15. 15. The article of claim 14 in which the vacuum deposited layer is a metal selected from the group consisting of chromium, stainless steel and aluminum and has a thickness of 200 A to 100
  16. 16. A metallised plastics article substantially as herein described or illustrated in the accompanying drawings.
GB51904/76A 1975-12-19 1976-12-13 Metallized flexible plastics automobile trimcomponent Expired GB1573008A (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US64254075A 1975-12-19 1975-12-19
US64256075A 1975-12-19 1975-12-19
US74585876A 1976-11-29 1976-11-29
US74585776A 1976-11-29 1976-11-29

Publications (1)

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GB1573008A true GB1573008A (en) 1980-08-13

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GB51904/76A Expired GB1573008A (en) 1975-12-19 1976-12-13 Metallized flexible plastics automobile trimcomponent

Country Status (9)

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JP (1) JPS5284266A (en)
AR (1) AR213943A1 (en)
AU (1) AU498861B2 (en)
DE (1) DE2656922C2 (en)
ES (2) ES454414A1 (en)
FR (2) FR2352666A1 (en)
GB (1) GB1573008A (en)
MX (1) MX145156A (en)
SE (1) SE438822B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0037235A2 (en) * 1980-03-25 1981-10-07 Ex-Cell-O Corporation An article of manufacture, such as an automobile trim component, comprising a dielectric substrate with a surface coating of metal and a process of manufacturing same
EP1084768A1 (en) * 1999-09-17 2001-03-21 Topy Kogyo Kabushiki Kaisha Bright Surface structure and a manufacturing method thereof

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0522170Y2 (en) * 1988-02-22 1993-06-07
US4911811A (en) * 1988-07-14 1990-03-27 The Stanley Works Method of making coated articles with metallic appearance
DE29819674U1 (en) 1998-11-04 1999-02-18 Schröter, Achim, 69221 Dossenheim interior panelling
KR100851660B1 (en) * 2008-03-18 2008-08-13 박성제 Metal ultra thin plate for a switch button device and preparing method the same
DE102012020872A1 (en) * 2012-10-24 2014-04-24 GM Global Technology Operations LLC (n. d. Ges. d. Staates Delaware) Motor car, has decorative element attached on support body and arranged in gusset of outer skin, where support body is injection-molded or extrusion-molded and comprises plastic vapor-deposited metal layer

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1068971B (en) * 1959-11-12 W. C. Heraeus Gesellschaft mit beschränkter Haftung, Hanau/M Process for metallizing objects made of polyethylene
US2993806A (en) * 1956-12-17 1961-07-25 Gen Tire & Rubber Co Metal coating of plastics
US3522074A (en) * 1965-06-28 1970-07-28 Minnesota Mining & Mfg Gold-plated high temperature sheet material
US3565743A (en) * 1965-06-28 1971-02-23 Minnesota Mining & Mfg Tape having a gold reflective surface attached to a glass fabric core and a pressure sensitive adhesive on the other surface

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0037235A2 (en) * 1980-03-25 1981-10-07 Ex-Cell-O Corporation An article of manufacture, such as an automobile trim component, comprising a dielectric substrate with a surface coating of metal and a process of manufacturing same
EP0037235B1 (en) * 1980-03-25 1987-03-11 Ex-Cell-O Corporation An article of manufacture, such as an automobile trim component, comprising a dielectric substrate with a surface coating of metal and a process of manufacturing same
EP1084768A1 (en) * 1999-09-17 2001-03-21 Topy Kogyo Kabushiki Kaisha Bright Surface structure and a manufacturing method thereof
US6767435B1 (en) 1999-09-17 2004-07-27 Topy Kogyo Kabushiki Kaisha Bright surface structure and a manufacturing method thereof

Also Published As

Publication number Publication date
AU2056376A (en) 1978-06-22
JPS569421B2 (en) 1981-03-02
DE2656922C2 (en) 1983-02-03
SE7614204L (en) 1977-06-20
FR2351783A1 (en) 1977-12-16
ES463470A1 (en) 1978-07-16
ES454414A1 (en) 1978-03-16
FR2352666A1 (en) 1977-12-23
JPS5284266A (en) 1977-07-13
AR213943A1 (en) 1979-04-11
FR2351783B1 (en) 1982-12-31
MX145156A (en) 1982-01-12
SE438822B (en) 1985-05-13
DE2656922A1 (en) 1977-06-30
AU498861B2 (en) 1979-03-29
FR2352666B1 (en) 1982-10-15

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