EP0324004A1 - Procede de preparation de blindage emi/rfi electrolaque en plastique - Google Patents
Procede de preparation de blindage emi/rfi electrolaque en plastiqueInfo
- Publication number
- EP0324004A1 EP0324004A1 EP88906496A EP88906496A EP0324004A1 EP 0324004 A1 EP0324004 A1 EP 0324004A1 EP 88906496 A EP88906496 A EP 88906496A EP 88906496 A EP88906496 A EP 88906496A EP 0324004 A1 EP0324004 A1 EP 0324004A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- plastic substrate
- conductive coating
- substrate
- electrocoated
- temperature
- 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.)
- Withdrawn
Links
- 239000004033 plastic Substances 0.000 title claims abstract description 68
- 229920003023 plastic Polymers 0.000 title claims abstract description 68
- 238000004519 manufacturing process Methods 0.000 title description 4
- 239000000758 substrate Substances 0.000 claims abstract description 138
- 238000000034 method Methods 0.000 claims abstract description 52
- 238000004070 electrodeposition Methods 0.000 claims abstract description 44
- 239000011248 coating agent Substances 0.000 claims abstract description 32
- 238000000576 coating method Methods 0.000 claims abstract description 32
- 239000003973 paint Substances 0.000 claims abstract description 26
- 238000007747 plating Methods 0.000 claims abstract description 23
- 229910052751 metal Inorganic materials 0.000 claims description 37
- 239000002184 metal Substances 0.000 claims description 37
- 238000007772 electroless plating Methods 0.000 claims description 18
- 229920002492 poly(sulfone) Polymers 0.000 claims description 13
- 229920000728 polyester Polymers 0.000 claims description 12
- 229920001778 nylon Polymers 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 239000004677 Nylon Substances 0.000 claims description 10
- 238000000151 deposition Methods 0.000 claims description 10
- 239000003054 catalyst Substances 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 8
- 229920000515 polycarbonate Polymers 0.000 claims description 8
- 239000004417 polycarbonate Substances 0.000 claims description 8
- 239000000956 alloy Substances 0.000 claims description 6
- 229910045601 alloy Inorganic materials 0.000 claims description 6
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 claims description 5
- 238000009713 electroplating Methods 0.000 claims description 4
- 238000005530 etching Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims 14
- 150000003512 tertiary amines Chemical class 0.000 claims 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 10
- 238000001723 curing Methods 0.000 description 9
- 230000008021 deposition Effects 0.000 description 8
- 238000007654 immersion Methods 0.000 description 8
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 6
- 229910052802 copper Inorganic materials 0.000 description 6
- 239000010949 copper Substances 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 229920006051 Capron® Polymers 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 3
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 3
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 3
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229910001369 Brass Inorganic materials 0.000 description 2
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 2
- 230000000712 assembly Effects 0.000 description 2
- 238000000429 assembly Methods 0.000 description 2
- 239000010951 brass Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000001746 injection moulding Methods 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000005022 packaging material Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- BALXUFOVQVENIU-KXNXZCPBSA-N pseudoephedrine hydrochloride Chemical compound [H+].[Cl-].CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 BALXUFOVQVENIU-KXNXZCPBSA-N 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- NGZXDRGWBULKFA-NSOVKSMOSA-N (+)-Bebeerine Chemical compound C([C@@H]1N(C)CCC=2C=C(C(=C(OC3=CC=C(C=C3)C[C@H]3C=4C=C(C(=CC=4CCN3C)OC)O3)C=21)O)OC)C1=CC=C(O)C3=C1 NGZXDRGWBULKFA-NSOVKSMOSA-N 0.000 description 1
- XEPXTKKIWBPAEG-UHFFFAOYSA-N 1,1-dichloropropan-1-ol Chemical compound CCC(O)(Cl)Cl XEPXTKKIWBPAEG-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910000979 O alloy Inorganic materials 0.000 description 1
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000005234 chemical deposition Methods 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001227 electron beam curing Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- -1 i.e. Substances 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000011415 microwave curing Methods 0.000 description 1
- 239000012811 non-conductive material Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000012970 tertiary amine catalyst Substances 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 229960004319 trichloroacetic acid Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D13/00—Electrophoretic coating characterised by the process
- C25D13/20—Pretreatment
Definitions
- This invention relates to EMI/RFI shielding in general and, more particularly, to decorative, EMI/RFI shielded electrocoated plastic components for electronic systems.
- EMI/RFI shielding is required by many electronic systems to absorb or reflect electromagnetic and radio frequency emissions. Such shielding is generally in the form of metal enclosures around electronic assemblies or subassemblies. For aesthetic reasons, it is often desirable to paint such enclosures.
- Electrocoating is one method which is used for applying a decorative coat of paint onto such metal enclosures.
- a metal substrate is immersed in an electrocoating solution and an organic resin, i.e., paint, is electrolytically deposited onto the metal substrate.
- Electrocoating solutions are typically a ⁇ ? ⁇ -ous emulsions of an electrocoating paint.
- the paint comprises a particular resin system, such as an epoxy, acrylic, or polyester system, along with cross-linking agents, such as melamine or blocked isocyanates, and solvents, pigments, and fillers.
- a solubilizing agent is present which combines with the resin particles to impart an electrical charge on the surface of the resin particle.
- the solubilizing agent acts as a dispersant to disperse the particles in the water and thereby form a stable emulsion.
- the metal substrate is immersed in the electrocoating composition, and a potential is established between the substrate and another electrode immersed in the composition.
- the substrate may be made either anodic or cathodic to the other electrode.
- the charged colloidal paint particles migrate toward and deposit on the metal substrate.
- the colloidal paint particles deposit and form a nonconductive film over the surface of the substrate. Because the film is nonconductive, the plating rat slows as the film thickness builds up and, when particular thickness is achieved, no further depositio occurs at that location. Deposition continues, -however, at other locations until the same thickness is achieved. Accordingly, a uniform thickness is eventually achieve over the entire substrate. Following deposition of the electrocoating paint, the substrate is rinsed and then baked in an oven a high temperatures to cure the paint. Such curin typically .requires a temperature of at least abou 300 ⁇ F.
- the present invention provides a process for makin plastic EMI/RFI shielded electrocoated components fo electronic systems and the like.
- the process comprise first electrolessly plating a plastic substrate t establish a conductive surface over the substrate
- Electroless deposition is followed by cathodicall electrocoating the plated substrate.
- substrate is then subjected to a curing step to cure th electrocoated paint.
- a injection-molded, three-dimensional, plastic substrat In a preferred embodiment of the invention, a injection-molded, three-dimensional, plastic substrat
- . is processed through an electroless plating proces wherein the substrate is first mounted on a platin rack, then immersed in a chemical etchant solution, the a catalyst solution, and finally an electroless platin solution.
- a chemical etchant solution such as copper or nickel
- electroless platin solution conductive layer of metal, such as copper or nickel, chemically deposits over the surface of the substrate.
- the electrolessly plated substrate is then mounte on a electrolytic plating rack such that the meta contacts of the plating rack are in electrical contac with the electrolessly plated conductive layer.
- Th mounted substrate is then immersed in an electrocoatin solution. A current is established between th substrate and an anode immersed in the bath, an electroating paint is electrolytically deposited to uniform thickness over the entire electrolessly plate surfac .
- the electrocoated substrate is then heated to temperature and for a time sufficient to cure th electrocoated paint without thermally deforming th plastic substrate or causing a loss of adhesion betwee the electrolessly deposited conductive layer and th substrate surface.
- the present invention provides a process particularly applicable to the manufacture of lightweight, decorative EMI/RFI shielded, three- 5 dimensional, plastic components for electronic systems.
- Such shielding components typically form enclosures around electronic assemblies or subassembl es- ⁇ > and -reflect and/or absorb electromagnetic and radio frequency emissions, whether generated by the electronic 0 assembly or subassembly, or by some outside source.
- the process comprises first providing a three- dimensional plastic substrate in the desired shape.
- the substrate is preferably formed by injection-molding and is made of a platable plastic material.
- the plastic 5 material may be any suitable plastic which is thermally stable at the temperature at which the applied electrocoated paint is cured.
- Preferred platable plastics include nylons, polyesters, polysul ones, and ABS-polysulfone alloys, polycarbonates and polycarbonate 0 alloys.
- the formed platable plastic substrate is mounted on a suitable plating rack and then electrolessly plated, preferably by conventional techniques.
- the electroless plating processes described 5 in U.S. Patent Nos. 4,335,164; 4,309,462; and 4,315,045 to Dillard, et.al. and assigned to Crown City Plating Company of El Monte, California, are preferably employed.
- the nylon substrate is first 0 preconditioned by immersion in an aqueous alkali metal hydroxide solution having a pH of at least about 10 and a temperature of about 150 ⁇ F, and preferably about 185°F.
- the substrate is then etched by immersion in a solution containing an organic acid, preferably tri- 5 chloroacetic acid.
- the substrate is seeded with a metal electroless plating catalyst, suc as that described in U.S. Patent No. 3,011,920 to C.R. Shipley, Jr. If required, the substrate is then • immersed in an activating solution to activate the catalyst, and then immersed in an electroless plating solution wherein metal, preferably copper or nickel, deposits onto the catalyzed surface of the substrate.
- the polyester substrate is optionally first contacted with a detergent rinse, followed by immersion in a hydrolyzer solution containing, for example, 350 grams per liter of chromic acid and 140 millimeters per liter of sulfuric acid, and maintained at a temperature of about 100°F to about 185°F.
- the polyester substrate is then conditioned by contact with an alkaline conditioner having a pH of at least 8 and maintained a a temperature of at least 135°F.
- the substrate is then contacted with " an aqueous acid fluoride etch having a pH less than abou 5 and a fluoride concentration of at least about 1 mole per liter.
- the fluoride etch is preferably maintained at a temperature from about 125°F to about 150 ⁇ F.
- the etched polyester substrate is then catalyzed and electrolessly plated generally as described above.
- an electroless plating process as described in U.S. Patent No. 4,125,649 to Donovan et al., assigned to Crown City Plating Company, is preferably employed.
- the substrate is first contacted with a chromic acid/sulfuric acid hydrolyzer solution as described above, followed by immersion in a pre-etch conditioner containing chlorinated compounds, such as dichloropropanol.
- the conditioner is maintained at a temperature of from about
- the substrate is then immersed in
- an etchant preferably a chromic acid etchant as described in U.S. Patent No. 3,668,130 to Kadison et al., assigned to Crown City Plating Company.
- the substrate " is rinsed, immersed in an " " alkaline cleanser, and then catalyzed and electrolessly plated as described above.
- ABS acrylonitrile butadiene styrene
- polycarbonates such as acrylonitrile butadiene styrene (ABS) and polycarbonates.
- ABS acrylonitrile butadiene styrene
- Such plastics are electrolessly plated, for example, according to the processes described in U.S. Patent Nos. 3,668,130 to
- Re-racking the substrate onto a plating rack is generally not preferred because of the added handling of the substrate which increases the rejection rate due to accidental marring, fingerprints, and the like. Also, the increased labor and the need for an additiona plating rack increases the cost of processing.
- points of contact between the first plating rack and th substrate are in recesses which entrap air when immerse in the various treating solutions, including th electroless plating solution. Such recesses do not ge electrolessly plated. Without re-racking, the meta contacts of the rack would not be in electrical contac with the conductive electroless plate which deposit over other areas of the substrate. Such electrica contact is required in the electrocoating step.
- re-racking may simply b desirable.
- many electroless plating rack are uncoated and therefore plate during the electroles plating process.
- Such racks are coated during th electrocoating process. This, of course, waste electrocoating material and makes the racks difficult to strip.
- a coated plating rack is used, i.e. one coated with * a nonconductive material except for the contacts, metal often- ' deposits on the coating material during the electroless plating process. If the deposited metal is in electrical communication with the metal contacts of the rack, the deposited metal will be electrocoated. Again, this wastes electrocoating material and makes the racks difficult to strip.
- the electrolessly plated substrate is suitably racked, it is then immersed in an electrocoating solution.
- a voltage is established between the substrate and one or more electrodes also immersed in the solution. The voltage is sufficient to cause the deposition of charged organic resin components onto the substrate.
- the electrocoated substrate is removed, rinsed with water and dried, preferably with an air gun.
- the electrocoated substrate is then subjected to a curing step, preferably baking at a temperature and for a time sufficient to cure the electrocoated paint, yet insufficient to warp the plastic substrate or cause any loss of adhes ⁇ on- between, the substrate " ''and - the -electrolessly deposited metal layer, or between the metal layer and the electrocoated layer.
- a curing step preferably baking at a temperature and for a time sufficient to cure the electrocoated paint, yet insufficient to warp the plastic substrate or cause any loss of adhes ⁇ on- between, the substrate " ''and - the -electrolessly deposited metal layer, or between the metal layer and the electrocoated layer.
- a curing step preferably baking at a temperature and for a time sufficient to cure the electrocoated paint, yet insufficient to warp the plastic substrate or cause any loss of adhes ⁇ on- between, the substrate " ''and - the -electrolessly deposited metal layer, or between the metal
- the electrocoating solution may be based on any suitable system, including acrylic, polyester, epoxy, and urethane systems. Currently, it is preferred to use an epoxy-based system as curing temperatures, for epoxy-based systems tend to be lower than for of other systems.
- the presently preferred electrocoating solution is manufactured by PPG Industries under the trade name PowerCron R 650.
- Such an electrocoating solution is an epoxy-based solution which requires a curing temperature of about 250°F.
- cathodic electrocoating solutions avoid electrolytic dissolution of the electrolessly deposited metal on the surface of the substrate. That is, if an anodic electrocoating solution is used when a voltage is established to make the substrate anodic, electrolessly deposited metal on the surface of the substrate will dissolve as the charged electrocoating particles deposit. Because the electroless layer is thin, such metal dissolution could cause a loss of conductivity which, in turn, could prevent an adequate buildup in the thickness of the electrocoated paint and possibly prevent deposition of the electrocoating paint entirely.
- the electrolessly plated substrate may be electrolytically plated prior to electrocoating.
- Such an additional step in the process may be desirable in certain cases.
- the electrolytic deposition of metal over the electroless layer would allow the overall thickness of the metal to buildup sufficiently to avoid any problems created by the use of an anodic electrocoating solution.
- the electrolytically deposited metal may be any suitable metal or combination of metals. Copper or a layer of copper followed by a layer of nickel is presently pref rred.
- a clear electrocoated paint over a decoratively plated plastic substrate.
- a decorative plate typically comprises one or more layers of electrolytically deposited metal over the electrolessly deposited layer.
- the final electrolytic layer e.g. gold, brass, chrome, etc. , imparts the desired appearance to the part, and the underlying layers, if used, impart desired physical properties, such as corrosion resistance, smoothness or leveling, ductility, and the like.
- While the presently preferred method of curing is by baking at a suitable temperature, it is also understood that other methods may be used. The suitability of other methods depend upon many factors, including-ithe -particular-*"electrocoating--solution -used, the size and shape of the substrate, and the availability of equipment. For example, ultraviolet light, electron beam, or microwave curing may be suitable in some applications. If a polyurethane system, involving the reaction of a polyol and an isocyanate is used, curing may be accomplished by contact of the electrocoated substrate with a gaseous tertiary-amine catalyst, as described, for example, in U.S. Patent Nos.
- Electrocoated plastic substrates offer numerous advantages over conventional electrocated metal substrates. Plastic substrates are much lighter, and the material tends to be less expensive than corresponding metal substrates. Moreover, complex shapes are often easier to produce by injection-molding than by conventional casting or other metal fabrication techniques. Because electroless processes involve chemical deposition rather than electrolytic deposition, complex shapes typically do not create problems with respect to coverage of the electrolessly deposited metal. That is, metal deposition over all areas of the substrate in contact with the electroless plating solution occurs whether those areas are high- current density or low-current density areas. This enables electrocoating over the entire surface of the substrate plated in the electroless process. Moreover, the deposited electroless layer provides sufficient conductivity so that the electrocoated substrates can be used as EMI/RFI shielding, if so desired.
- the process of first applying a conductive electroless layer followed by a nonconductive electrocoated layer may be repeated, if desired, one or more times to yield a laminate or sandwich effect.
- the substrate was rinsed and immersed in an etch solution containing about 15% trichloracetic acid at ambient temperature.
- the substrate was then rinsed and immersed in the second sodium hydroxide solution containing 150g/l sodium hydroxide and maintained at 150"F for about 1 minute.
- the article was then immersed in an acid solution containing 4% fluoboric acid at about 125DF for about 1 minute.
- the substrate was then catalyzed by immersion for about 60 seconds in a colloidal palladium catalyst manufactured by The Shipley Company under the trade name Cataposit PM 958.
- the catalyst solution was maintained at about 120 ⁇ F.
- the substrate was then immersed in an acid accelerator to expose the palladium metal.
- the accelerator contained 4% fluoboric acid ..and .was maintained at about 120"F.
- Contact time was for about 120 seconds.
- the substrate then was electrolessly plated by immersion in a nickel electroless plating solution sold by The Shipley Company under the trade name Niposit PM 980. Immersion time was about 420 seconds, and the temperature of the solution was about 80*F.
- the substrate was then rinsed and dried.
- the substrate was removed from the electroless plating rack and mounted on an electrolytic plating rack.
- the substrate was then cleaned by immersion in an alkaline soak cleaner.
- the cleaned substrate was then .electrolytically plated with copper for twenty minutes at about 2 volts.
- the plated substrate was then rinsed and dried.
- the electrolytically plated substrate was then racked onto a steel non-coated rack and immersed in a cathodic acrylic electrocoating solution sold under the trade name PowerCron s 650 by PPG Industries.
- the electrocoating solution was maintained at a temperature of 76" to 78°F, and a voltage was established of 75 to 100 volts. Electrocoating continued for one minute.
- the electrocoated part was then rinsed, blown dry wit an air gun, and baked for twenty minutes at 250"F to cure the electrocoated paint.
- EXAMPLE 2 A hub cap made of Capron 8260 resin, a mineral filled nylon manufactured and sold by Allied Corp., wa electrolessly plated by the process described in Exampl 1.
- the electrolessly plated substrate was then racke onto a steel non-coated rack and immersed in the sam electrocoating solution as described in Example 1, i.e., a cathodic acrylic electrocoating solution sold unde the trade name PowerCron 650 by PPG Industries.
- the electrocoating solution was maintained at a temperature of about 80" A F, and a voltage was established of 125 volts for 30 seconds and was then increased to 150 volts for an additional 15 seconds.
- the electrocoated part was then rinsed, blown dry with an air gun, and baked for twenty minutes at 270° A F to " cure the electrocoated paint.
- the electrolyti ⁇ ally plated substrate was then racked onto a steel non-coated rack and immersed in a cathodic acrylic electrocoating solution sold under the trade name PowerCron 650 by PPG Industries.
- the electrocoating solution was maintained at a temperature of about 85DF, and a voltage was established of about 150 volts. Electrocoating continued for one minute.
- the electrocoated part was then rinsed, blown dry with an air gun, and baked for twenty minutes at 270DF to cure the electrocoated paint.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemically Coating (AREA)
Abstract
Procédé d'électrolaquage de substrats en plastique consistant à monter le substrat en plastique sur un montage porte-pièce et ensuite à galvaniser le substrat sans courant. Ensuite on monte le substrat galvanisé sans courant sur un second montage porte-pièce et on l'immerge dans une solution d'électroplaquage cathodique dans laquelle une couche de peinture non conductrice se dépose sur le substrat. Puis on durcit la couche de peinture non conductrice par cuisson à une température suffisante pour durcir la couche, mais insuffisante pour provoquer une déformation du substrat.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6793687A | 1987-06-29 | 1987-06-29 | |
| US67936 | 1998-04-28 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0324004A1 true EP0324004A1 (fr) | 1989-07-19 |
| EP0324004A4 EP0324004A4 (fr) | 1989-12-13 |
Family
ID=22079389
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP19880906496 Withdrawn EP0324004A4 (fr) | 1987-06-29 | 1988-06-29 | Procede de preparation de blindage emi/rfi electrolaque en plastique. |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP0324004A4 (fr) |
| WO (1) | WO1989000075A1 (fr) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0416338A (ja) * | 1990-05-09 | 1992-01-21 | C Uyemura & Co Ltd | 電磁波シールド層の形成方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3558290A (en) * | 1968-04-02 | 1971-01-26 | Union Carbide Corp | Plated plastic printing plates |
| US4368222A (en) * | 1981-06-05 | 1983-01-11 | Ashland Oil, Inc. | Vapor permeation curable coatings for surface-porous substrates |
| JPS6289898A (ja) * | 1985-10-15 | 1987-04-24 | C-Ren Kk | 繊維布帛の加工方法 |
-
1988
- 1988-06-29 WO PCT/US1988/002219 patent/WO1989000075A1/fr not_active Ceased
- 1988-06-29 EP EP19880906496 patent/EP0324004A4/fr not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| EP0324004A4 (fr) | 1989-12-13 |
| WO1989000075A1 (fr) | 1989-01-12 |
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