US3390061A - Protective localized area resin coatings for electroplating - Google Patents

Protective localized area resin coatings for electroplating Download PDF

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Publication number
US3390061A
US3390061A US543070A US54307066A US3390061A US 3390061 A US3390061 A US 3390061A US 543070 A US543070 A US 543070A US 54307066 A US54307066 A US 54307066A US 3390061 A US3390061 A US 3390061A
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resin
electroplating
metal
protective
coating
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US543070A
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Levinos Steven
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GAF Chemicals Corp
Eastman Kodak Co
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General Aniline and Film Corp
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Publication date
Priority to NL133909D priority Critical patent/NL133909C/xx
Application filed by General Aniline and Film Corp filed Critical General Aniline and Film Corp
Priority to US543070A priority patent/US3390061A/en
Priority to US562466A priority patent/US3451902A/en
Priority to NL6705209A priority patent/NL6705209A/xx
Priority to DE1967G0049849 priority patent/DE1621081B1/en
Priority to FR103031A priority patent/FR1521734A/en
Priority to GB07588/67A priority patent/GB1172765A/en
Application granted granted Critical
Publication of US3390061A publication Critical patent/US3390061A/en
Assigned to EASTMAN KODAK COMPANY, A CORP. OF NJ. reassignment EASTMAN KODAK COMPANY, A CORP. OF NJ. ASSIGNMENT OF ASSIGNORS INTEREST. Assignors: GAF CORPORATION
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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41NPRINTING PLATES OR FOILS; MATERIALS FOR SURFACES USED IN PRINTING MACHINES FOR PRINTING, INKING, DAMPING, OR THE LIKE; PREPARING SUCH SURFACES FOR USE AND CONSERVING THEM
    • B41N1/00Printing plates or foils; Materials therefor
    • B41N1/04Printing plates or foils; Materials therefor metallic
    • B41N1/08Printing plates or foils; Materials therefor metallic for lithographic printing
    • B41N1/10Printing plates or foils; Materials therefor metallic for lithographic printing multiple
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D133/00Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
    • C09D133/04Homopolymers or copolymers of esters
    • C09D133/06Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
    • C09D133/08Homopolymers or copolymers of acrylic acid esters
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/02Electroplating of selected surface areas
    • C25D5/022Electroplating of selected surface areas using masking means

Definitions

  • the present invention relates in general to protective coatings and more particularly to resin-based protective coatings advantageously adapted for use in connection with coating operations requiring the deposition of metal upon metal.
  • the feasibility of a given coating method will depend, inter alia, upon the type of metal serving a the base material, the type of coating to be deposited, the physical extent of the metallic film to be deposited, i.e., whether all or only certain pre-selected surfaces of the base material are to be coated. In those instances wherein the entire surface area of the metallic article is to be coated, i.e., wherein complete immersion of the metallic article in the plating bath is indicated, it is quite likely that any of the conventional coating techniques promulgated for such purposes is eminently applicable.
  • the industrial applications are legion wherein metal on metal deposition is desirably effected upon only certain and pre-selected surfaces of the metallic article.
  • the particular application may require that only certain discrete areas of a given metal surface be so coated as would be the case for example when providing ornamental or decorative designs.
  • coating techniques which require immersing the entire metallic article in the plating medium, e.g., electroplating, would not be feasible in the absence of some manipulative technique designed to locally immunize such metallic article against the effects of the plating medium.
  • a Wide variety of techniques have been evolved in the art by which such localized immersion can be accomplished.
  • Paramount among the manipulative techniques thus far evolved in this regard are those based upon the use of protective coatings of a temporary nature, i.e., temporary in the sense of being unaffected by prolonged contact with the solution media employed in the coating operation but which are nevertheless easily removed by suitable postcoating treatment.
  • such protective coating compositions contain as the essential ingredient a filmforming, polymeric resinous material, either natural or synthetic, capable of forming a strong, adhesive bond with the metal article being coated.
  • a further source of difficulty stems from the fact that many of the resin materials currently employed for the aforedescribed purposes exhibit undesirable change in solubility characteristics as a result of prolonged immersion in the plating bath to the extent that complete removal of the protective resin coating from the metal surface is rendered extremely difficult.
  • the latter phenomena often necessitates resort to mechanical, e.g. abrading as opposed to purely chemical, i.e., solubilization techniques to assure such removal.
  • Such techniques are in most instances burdensome both from the standpoint of economics as well as ease of processing.
  • Such printing plates comprise for example an aluminum base provided on one side with a surface coating of copper, chromium or the like, such surface coating serving as the support for a light-sensitive, resist-forming layer.
  • An integral phase in the processing of such sensitized elements involves the etching out of the surface metal coating, this being accomplished pursuant to the provision of a final plate having grease-repellent and grease-receptive areas.
  • the techniques heretofore provided for the preparation of such bimetallic base plates have left much to be desired.
  • a primary object of the present invention resides in the provision of improved, resin-containing protective coatings admirably suited for use in connection with metal to metal coating operations and wherein. one or more of the surfaces of such metal is to be protected against the plating medium.
  • Another object of the present invention resides in the provision of improved resin-containing protective coatings of a temporary nature advantageously adapted for use in connection with the preparation of bimetallic plates and wherein such resin is completely unaffected by the metal plating medium, e.g., the electrolytic plate bath; forms an adhesion bond of exceptional strength with the metal being coated; and is capable of being easily and completely removed from the metal surface subsequent to the plating operation.
  • the metal plating medium e.g., the electrolytic plate bath
  • thermoplastic, film-forming, acrylic resins which are soluble in alkaline media, i.e., a pH ranging from approximately 7.5 to 8.0, as the protective coating material in metal to metal coating techniques.
  • the protective resin coating can be easily removed by treating same with an alkaline media, e.g., an ammonium hydroxide solution having a pH ranging from 7.5 to 8.0.
  • an alkaline media e.g., an ammonium hydroxide solution having a pH ranging from 7.5 to 8.0.
  • alkaline-soluble resin materials contemplated for use herein are derived from such monomers as acrylic acid, methacrylic acid, methyl methacrylate, etc., i.e., alpha, beta-ethylenically unsaturated carboxylic acids, their esters, hydrolysis products and their salts. Particularly beneficial results in terms of strength of adhesion as well as overall structural stability under the conditions employed for plating an aluminum sheet with copper, chromium, etc.
  • the resin is applied in the form of an 0.5 to 1% solution in isopropyl alcohol, although other solvents such as methanol, ethanol, acetone, diacetone alcohol, methyl Cellosolve, dioxane, cyclohexanol, ethyl acetate, and the like may be used.
  • solvents such as methanol, ethanol, acetone, diacetone alcohol, methyl Cellosolve, dioxane, cyclohexanol, ethyl acetate, and the like may be used.
  • oleic acid and a surface-active agent such as Alkaterge A is advantageous in promoting uniform Wetting when the resin is applied to the metal surface.
  • the protective resin coating compositions of the present invention may be advantageously employed in any metal to metal coating operation requiring complete immersion of the metal to be coated in the plating medium, they have particularly advantageous applicability to electroplating operations involving the deposition of copper or chromium upon aluminum.
  • EXAMPLE I This example illustrates the application of the present invention to the production of a copper-coated aluminum plate.
  • EXAMPLE H A resin pre-eoated aluminum sheet is prepared in the manner described in Example I. Copper plating of the coated aluminum surface is carried out with the following plating solution utilizing the parameters indicated:
  • Copper fluoborate gms. 224 Fluoboric acid gms. 15 Boric acid gms. 15 Water to make liter 1 Cathode current density amps. per sq. ft. 35 Anode current density amps. per sq. ft. 30 Temperature, F.
  • the pH of the above solution is approximately 1.4.
  • the aluminum cathode is removed from the bath and given a Water rinse. Removal of the protective resin coating is accomplished in the manner described in Example I. Similar results are obtained in terms of ease of resin removal as well as resistance of the protective resin to the effects of the plating medium.
  • the nature of the plating bath is likewise not a critical factorin the practice of the present invention, the sole requirement being that such bath be maintained under an acid pH and preferably below 6.5.
  • the subject invention may be applied to production of metal surfaces containing ornamental or decorative designs thereon.
  • the metal to be coated need not be planar but may be of arcuate or otherwise irregular configuration.
  • the resin may be suitably applied by the use of a suitable stencil, pattern, etc.
  • the procedure employed would be similar to that described in the above examples both as regards the electroplating operation and the protective resin removal operation.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Metallurgy (AREA)
  • Electroplating Methods And Accessories (AREA)
  • Manufacture Or Reproduction Of Printing Formes (AREA)

Description

United States Patent 3,390,061 PROTECTIVE LOCALIZED AREA RESIN COATINGS FOR ELECTROPLATING Steven Levinos, Vestal, N.Y., assignor to General Aniline & Film Corporation, New York, N.Y., a corporation of Delaware No Drawing. Filed Apr. 18, 1966, Ser. No. 543,070
4 Claims. (Cl. 204-) The present invention relates in general to protective coatings and more particularly to resin-based protective coatings advantageously adapted for use in connection with coating operations requiring the deposition of metal upon metal.
A wide variety of methods for effectuating metal to metal coating operations are, of course, Well known in the art being extensively described in the literature both patent and otherwise. The state of the art in this regard is such as to require little in the way of explanatory comment. Thus, it is common knowledge that the deposition H of metal upon metal can be carried out by implementation of a number of techniques including, for example, galvanic, i.e., electrodeposition, dip coating, etc. The particular method selected will, of course, depend upon a number of considerations with perhaps the paramount criteria relating to the nature of the coating desired. Otherwise stated, the feasibility of a given coating method will depend, inter alia, upon the type of metal serving a the base material, the type of coating to be deposited, the physical extent of the metallic film to be deposited, i.e., whether all or only certain pre-selected surfaces of the base material are to be coated. In those instances wherein the entire surface area of the metallic article is to be coated, i.e., wherein complete immersion of the metallic article in the plating bath is indicated, it is quite likely that any of the conventional coating techniques promulgated for such purposes is eminently applicable.
In contradistinction, the industrial applications are legion wherein metal on metal deposition is desirably effected upon only certain and pre-selected surfaces of the metallic article. Moreover, the particular application may require that only certain discrete areas of a given metal surface be so coated as would be the case for example when providing ornamental or decorative designs. As will be readily apparent, the utilization of coating techniques which require immersing the entire metallic article in the plating medium, e.g., electroplating, would not be feasible in the absence of some manipulative technique designed to locally immunize such metallic article against the effects of the plating medium. Heretofore, a Wide variety of techniques have been evolved in the art by which such localized immersion can be accomplished. Paramount among the manipulative techniques thus far evolved in this regard are those based upon the use of protective coatings of a temporary nature, i.e., temporary in the sense of being unaffected by prolonged contact with the solution media employed in the coating operation but which are nevertheless easily removed by suitable postcoating treatment. invariably, such protective coating compositions contain as the essential ingredient a filmforming, polymeric resinous material, either natural or synthetic, capable of forming a strong, adhesive bond with the metal article being coated.
Despite the relatively widespread commercial acceptance of methods based upon the employment of temporary protective resin coatings, considerable difficulty has nevertheless been encountered as regards the obtention of optimum results. In the main, the resinous materials thus far employed for such purposes are uniformly characterized in that they fail to provide the requisite measure of protection, i.e., metal surfaces coated therewith will usually exhibit some degree of metal deposition. As will Patented June 25, 1968 'ice be readily appreciated, it is of utmost importance that the protective resin coating be substantially, if not completely, impermeable to the plating bath in order to exclude even the remotest possibility of spurious metal deposition. Moreover, in many cases, it has been ascertained that the degree of adhesion extent between the resin coating and the metal surface tends to diminish to an intolerable extent, such a tendency being particularly manifest with the use of even moderately severe conditions of operation, e.g., temperature, period of immersion, solution corrosivity, etc.
A further source of difficulty stems from the fact that many of the resin materials currently employed for the aforedescribed purposes exhibit undesirable change in solubility characteristics as a result of prolonged immersion in the plating bath to the extent that complete removal of the protective resin coating from the metal surface is rendered extremely difficult. The latter phenomena often necessitates resort to mechanical, e.g. abrading as opposed to purely chemical, i.e., solubilization techniques to assure such removal. Such techniques are in most instances burdensome both from the standpoint of economics as well as ease of processing.
The foregoing situation has proved to be of special consequence in connection with the production of bimetallic plates contemplated for ultimate use in the photomechanical reproduction arts, i.e., the preparation of photomechanical printing plates. Conventionally, such printing plates comprise for example an aluminum base provided on one side with a surface coating of copper, chromium or the like, such surface coating serving as the support for a light-sensitive, resist-forming layer. An integral phase in the processing of such sensitized elements involves the etching out of the surface metal coating, this being accomplished pursuant to the provision of a final plate having grease-repellent and grease-receptive areas. However, as mentioned hereinbefore, the techniques heretofore provided for the preparation of such bimetallic base plates have left much to be desired.
Thus, a primary object of the present invention resides in the provision of improved, resin-containing protective coatings admirably suited for use in connection with metal to metal coating operations and wherein. one or more of the surfaces of such metal is to be protected against the plating medium.
Another object of the present invention resides in the provision of improved resin-containing protective coatings of a temporary nature advantageously adapted for use in connection with the preparation of bimetallic plates and wherein such resin is completely unaffected by the metal plating medium, e.g., the electrolytic plate bath; forms an adhesion bond of exceptional strength with the metal being coated; and is capable of being easily and completely removed from the metal surface subsequent to the plating operation.
Other objects and advantages of the present invention will become apparent as the description proceeds.
The attainment of the foregoing and related objects is made possible in accordance with the present invention which in its broader aspects relates to the use of thermoplastic, film-forming, acrylic resins which are soluble in alkaline media, i.e., a pH ranging from approximately 7.5 to 8.0, as the protective coating material in metal to metal coating techniques.
In accordance with the present invention, it has been ascertained that the use of such resins, and especially in coating operations involving the application of a metallic coating to one side of an aluminum base, leads to a considerable reduction in processing time as well as materials handling. For example, it has been found that resin materials of the aforedescribed type are completely known, such plating solutions are usually one of four types viz. copper cyanide, copper sulfate, copper fluoborate or copper pyrophosphate. Not only do such resin materials serve as effective diffusion barrier layers, but in addition, retain a firmly adherent bonding with the aluminum surface throughout the entire plating operation. Perhaps the salient advantage attending the use of such resin materials relates to their ready solubility in alkaline media. Thus, immediately following completion of the plating operation, e.g., electrodeposition of copper on aluminum, the protective resin coating can be easily removed by treating same with an alkaline media, e.g., an ammonium hydroxide solution having a pH ranging from 7.5 to 8.0.
The alkaline-soluble resin materials contemplated for use herein are derived from such monomers as acrylic acid, methacrylic acid, methyl methacrylate, etc., i.e., alpha, beta-ethylenically unsaturated carboxylic acids, their esters, hydrolysis products and their salts. Particularly beneficial results in terms of strength of adhesion as well as overall structural stability under the conditions employed for plating an aluminum sheet with copper, chromium, etc. are obtained with the resin materials commercially available and carrying the trade name designation Carboset, e.g., Carboset 5257 In general, the resin is applied in the form of an 0.5 to 1% solution in isopropyl alcohol, although other solvents such as methanol, ethanol, acetone, diacetone alcohol, methyl Cellosolve, dioxane, cyclohexanol, ethyl acetate, and the like may be used. The addition of a small quantity of oleic acid and a surface-active agent such as Alkaterge A is advantageous in promoting uniform Wetting when the resin is applied to the metal surface.
Although the protective resin coating compositions of the present invention may be advantageously employed in any metal to metal coating operation requiring complete immersion of the metal to be coated in the plating medium, they have particularly advantageous applicability to electroplating operations involving the deposition of copper or chromium upon aluminum.
The present invention Will be further illustrated by the following examples but it is to be understood that the invention is not restricted thereto.
EXAMPLE I This example illustrates the application of the present invention to the production of a copper-coated aluminum plate. An aluminum plate, the surfaces of which have been rendered oxide-free by dipping in sodium hydroxide solution, is flow-coated on one side with a protective coating comprising the following composition:
' Parts Carboset 525, 0.75% in isopropyl alcohol 98.0 Alkaterge A, 1% in isopropyl alcohol 1.0 Oleic acid, 2% in isopropyl alcohol 1.0
Approximately 5 cc. of the above composition is employed per sq. ft. of area to be coated. The coating is then allowed to dry for a period of about to minutes. The aluminum plate thus coated is immersed in a plating bath of the copper sulfate type, the aluminum serving as the cathode, the anode being an oxide-free, high-purity copper, with the uncoated aluminum surface facing the anode.
The conditions and parameters of the electroplating operation are summarized as follows:
Copper sulfate '5H O gms.u 200 Sulfuric acid gms. 70 Water to make liter 1 Cathode current density amps./ per sq. ft. Anode current density amps./ per sq. ft. 30 Bath temperature, F. 85/90 The plating operation is carried out for a period of approximately 3 minutes. The aluminum cathode is removed from the plating bath and given a water rinse.
Visual examination of the copper coated aluminum sheet revealed that the protective resin layer had remained intact throughout the entire electroplating treatment being totally unaffected by the plating solution. Furthermore, the adhesion of the resin coating to the aluminum surface is in no way deleteriously affected. Despite the strong adhesive bond, the protective resin coating is easily and completely removed from the aluminum surface by swabbing with a pad which has previously been dipped in an ammonium hydroxide solution having a pH of about 7.8. Resin removal is complete by the solvent-swabbing treatment to the extent that a polished aluminum surface is obtained merely by wiping with a cotton cloth. Thus, it is readily apparent that the alkaline solubility of the resin material remains unchanged despite subjection to the plating medium. The total time consumed in removing the protective resin coating is approximately 45 seconds.
EXAMPLE H A resin pre-eoated aluminum sheet is prepared in the manner described in Example I. Copper plating of the coated aluminum surface is carried out with the following plating solution utilizing the parameters indicated:
Copper fluoborate gms. 224 Fluoboric acid gms. 15 Boric acid gms. 15 Water to make liter 1 Cathode current density amps. per sq. ft. 35 Anode current density amps. per sq. ft. 30 Temperature, F.
The pH of the above solution is approximately 1.4.
After electrodeposition of the copper film on the unprotected aluminum surface is complete, i.e., after a period of approximately 3 minutes, the aluminum cathode is removed from the bath and given a Water rinse. Removal of the protective resin coating is accomplished in the manner described in Example I. Similar results are obtained in terms of ease of resin removal as well as resistance of the protective resin to the effects of the plating medium.
Results similar to those described in the above examples are obtained when utilizing a chromium plating bath maintained under an acid pH. It will be understood that the nature of the alkali employed in the resin-removal step is not particularly critical and accordingly, may be selected from a wide variety of materials, e.g., alkali metal hydroxides such as sodium hydroxide, potassium hydroxide, etc., trisodium phosphate and the like. The important consideration in this regard is that the resin-removal bat-h be maintained at an alkaline pH and preferably within a pH ranging from 7.5 to 8.
Moreover, the nature of the plating bath is likewise not a critical factorin the practice of the present invention, the sole requirement being that such bath be maintained under an acid pH and preferably below 6.5.
The subject invention may be applied to production of metal surfaces containing ornamental or decorative designs thereon. The metal to be coated need not be planar but may be of arcuate or otherwise irregular configuration. In such instances, the resin may be suitably applied by the use of a suitable stencil, pattern, etc. The procedure employed would be similar to that described in the above examples both as regards the electroplating operation and the protective resin removal operation.
The present invention has been disclosed with respect to certain preferred embodiments thereof, and there will become obvious to persons skilled in the art various modifications, equivalents or variations thereof which are intended to be included within the spirit and scope of this invention.
What is claimed is:
1. The process of electroplating an aluminum sheet with a metal selected from the group consisting of copper and chromium, said electroplating being carried out at an acid pH, the improvement which comprises employing as the cathode an oxide-free aluminum sheet having coated thereon a localized area protective resin layer selected from the group consisting of thermoplastic, film-forming acrylic resins soluble in alkaline media, said resin being capable of forming a strong, adhesive bond with the aluminum surface and wherein said resin is capable of being completely removed from the aluminum surface subsequent to the electroplating operation by subjecting same to an alkaline medium maintained at a pH of at least 7.5.
2. The process according to claim 1 wherein said resin comprises an acrylic acid polymer.
3. The process according to claim 1 wherein said resin comprises a partially hydrolyzed acrylate polymer.
4. The process according to claim 1 wherein said electroplating is carried out at elevated temperatures.
References Cited UNITED STATES PATENTS 2,951,019 8/1960 Dalton 2O4-17 2,999,771 9/1961 Gaynes 204-45 3,l21,009 2/1964 Giaimo 204-18 10 JOHN H. MACK, Primary Examiner.
T. T-UFARIELLO, Assistant Examiner.

Claims (1)

1. THE PROCESS OF ELECTROPLATING AN ALUMINUM SHEET WITH A METAL SELECTED FROM THE GROUP CONSISTING OF COPPER AND CHROMIUM, SAID ELECTROPLATING BEING CARRIED OUT AT AN ACID PH, THE IMPROVEMENT WHICH COMPRISES EMPLOYING AS THE CATHODE AN OXIDE-FREE ALUMINUM SHEET HAVING COATED THEREON A LOCALIZED AREA PROTECTIVE RESIN LAYER SELECTED FROM THE GROUP CONSISTING OF THERMOPLASTIC, FILM-FORMING ACRYLIC RESINS SOLUBLE IN ALKALINE MEDIA, SAID RESIN BEING CAPABLE OF FORMING A STRONG, ADHESIVE BOND WITH THE ALUMINUM SURFACE AND WHEREIN SAID RESIN IS CAPABLE OF BEING COMPLETELY REMOVED FROM THE ALUMINUM SURFACE SUBSEQUENT TO THE ELECTROPLATING OPERATION BY SUBJECTING SAME TO AN ALKALINE MEDIUM MAINTAINED AT A PH OF AT LEAST 7.5.
US543070A 1966-04-18 1966-04-18 Protective localized area resin coatings for electroplating Expired - Lifetime US3390061A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
NL133909D NL133909C (en) 1966-04-18
US543070A US3390061A (en) 1966-04-18 1966-04-18 Protective localized area resin coatings for electroplating
US562466A US3451902A (en) 1966-04-18 1966-07-05 Protective localized area resin coatings for electroplating
NL6705209A NL6705209A (en) 1966-04-18 1967-04-13
DE1967G0049849 DE1621081B1 (en) 1966-04-18 1967-04-17 Cover varnish for the partial electroplating of aluminum in acidic copper or chrome baths
FR103031A FR1521734A (en) 1966-04-18 1967-04-17 Localized electrolytic plating of metals in the presence of protective resin layers
GB07588/67A GB1172765A (en) 1966-04-18 1967-04-17 Improvements in or relating to Electroplating Aluminium with Copper or Chromium

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Application Number Priority Date Filing Date Title
US543070A US3390061A (en) 1966-04-18 1966-04-18 Protective localized area resin coatings for electroplating
US56246666A 1966-07-05 1966-07-05

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US562466A Expired - Lifetime US3451902A (en) 1966-04-18 1966-07-05 Protective localized area resin coatings for electroplating

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3862875A (en) * 1971-03-17 1975-01-28 Micro Science Associates Filler masking of small apertures
US4994349A (en) * 1988-06-27 1991-02-19 At&T Bell Laboratories Printed wiring board fabrication method
CN101301631B (en) * 2008-01-23 2013-06-05 四川大学 Method for preparing protective coating of catalytic converter for purifying motorcycle tail gas during electroplating process

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2512086C3 (en) * 1975-03-19 1978-11-30 Siemens Ag, 1000 Berlin Und 8000 Muenchen Process for the production of self-supporting, thin metal structures
US4224118A (en) * 1979-09-04 1980-09-23 General Motors Corporation Method of masking plated article with a poly(isobutyl methacrylate) and poly(vinyl toluene) containing coating
US4834821A (en) * 1988-01-11 1989-05-30 Morton Thiokol, Inc. Process for preparing polymeric materials for application to printed circuits
US5567482A (en) * 1995-12-20 1996-10-22 Usx Corporation Method of protecting steel strip
US5800695A (en) * 1996-10-16 1998-09-01 Chromalloy Gas Turbine Corporation Plating turbine engine components
US20050151129A1 (en) 2004-01-14 2005-07-14 Rahul Gupta Deposition of conducting polymers
DE102011011200A1 (en) 2011-02-14 2012-08-16 Dechema Gesellschaft Für Chemische Technik Und Biotechnologie E.V. Producing a metal edge zone of a metal component enriched with at least one additional element comprises inward diffusion of the additional elements from a metal film in the metallic substrate, surrounding the component

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2951019A (en) * 1953-06-09 1960-08-30 Harold R Dalton Method of making plated intaglio printing form
US2999771A (en) * 1958-04-17 1961-09-12 Norman I Gaynes Chrome plating and anodizing stopoff composition
US3121009A (en) * 1960-03-16 1964-02-11 Rca Corp Preparation of etched plates

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2951019A (en) * 1953-06-09 1960-08-30 Harold R Dalton Method of making plated intaglio printing form
US2999771A (en) * 1958-04-17 1961-09-12 Norman I Gaynes Chrome plating and anodizing stopoff composition
US3121009A (en) * 1960-03-16 1964-02-11 Rca Corp Preparation of etched plates

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3862875A (en) * 1971-03-17 1975-01-28 Micro Science Associates Filler masking of small apertures
US4994349A (en) * 1988-06-27 1991-02-19 At&T Bell Laboratories Printed wiring board fabrication method
CN101301631B (en) * 2008-01-23 2013-06-05 四川大学 Method for preparing protective coating of catalytic converter for purifying motorcycle tail gas during electroplating process

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DE1621081B1 (en) 1971-04-22
NL133909C (en)
GB1172765A (en) 1969-12-03
NL6705209A (en) 1967-10-19
US3451902A (en) 1969-06-24

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