US3699017A - Polar activating particles for electrodeposition process - Google Patents

Polar activating particles for electrodeposition process Download PDF

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Publication number
US3699017A
US3699017A US147409A US3699017DA US3699017A US 3699017 A US3699017 A US 3699017A US 147409 A US147409 A US 147409A US 3699017D A US3699017D A US 3699017DA US 3699017 A US3699017 A US 3699017A
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Prior art keywords
particles
particle
conductive
sheath
electrolyte
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US147409A
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English (en)
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Steve Eisner
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Saint Gobain Abrasives Inc
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Norton Co
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    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/22—Electroplating combined with mechanical treatment during the deposition
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
    • C25D5/60—Electroplating characterised by the structure or texture of the layers
    • C25D5/605—Surface topography of the layers, e.g. rough, dendritic or nodular layers
    • C25D5/611—Smooth layers

Definitions

  • the conductive mass and/or the outer sheath is so formed or treated that the conductive mass does not protrude beyond the sheath at any of said openlngs.
  • the present invention relates to electrodeposition of metal onto a substrate from a liquid electrolyte solution by imposed current flow. It is particularly adapted for use in a system such as those disclosed and claimed in the copending applications of Steve Eisner, Ser. No. 102,287, filed Dec. 29, 1970 and of Norvell E. Wisdom, In, Ser. No. 140,143, filed May 4, 1971 (which are more fully described below).
  • Particulate material of various kinds has heretofore been incorporated into plating baths, generally with the idea that it would polish or densify plate laid down by conventional means and at conventional rates.
  • this material has been incorporated in the form of a suspension with agitation of the liquid electrolyte serving to keep this material suspended therein.
  • the particles were relatively large and motion of the container served to cause these materials to beat or pound the plate after it was deposited to densify the plate.
  • an extremely low particle to liquid volume ratio was employed.
  • French 1,500,269 recognized that incorporating a relatively high volume of particles to liquid in the form of a fluidized bed caused a reduction in cell voltage at constant relatively low current densities in a specialized plating system as compared with the voltage resulting from high flow rates of electrolyte only.
  • This patent also suggests that conductive particles could be used if desired.
  • Conductive particles have also been used to form fluidized bed electrodes in work sponsored by the National Research and Development Council in Great Britain. Still more recently, the aforementioned processes described and claimed in US. applications, Ser. Nos.
  • the processes of Ser. Nos. 102,287 and 140,143 in which the present invention is particularly applicable generally rely on activating the surface of an electrodeposit by repeated contacts over very short time intervals with a plurality of small dynamically hard particles.
  • Activating the surface means so treating the surface as to create at such surface a high tendency to utilize the imposed current to deposit metal in sound, adherent form rather than as powder or dendrites.
  • Dynamically hard is defined to mean that the particles act, through a combination of their actual hardness, mass, impact speed and pressure, in such a manner as to activate the electrodeposit surface and generally a criteria of this hardness is the formation in the surface of the deposit of visible scratch patterns (visible at least under a magnification of 10,000X or less).
  • the particles are placed in a container capable of being vibrated by externally imposed forces which imparts both a macroand a micro-motion to such particles as a result of impacts between such particles and the walls of the container.
  • Electrolyte is placed in such container along with the particles with the electrolyte level being above or at least substantially filling the plating zone in the case of the process of Ser. No. 102,287 and below or just barely into such zone in the case of the process of Ser. No. 140,143.
  • Motion is initiated in each instance before any current flow is imposed and such motion is continued throughout the plating cycle.
  • the cathodic part being plated is fixtured in the container although it can be arranged so as to move therethrough in a predetermined and fixed path.
  • the particles are entirely or at least predominately non-conductive electrically. It is possible, as disclosed in these aforementioned applications, to use a small amount, i.e., up to about 5% by volume of conductive partlc es along with the major portion of non-conductive particles.
  • the present invention is directed to a type of conductive particle which can be used as the sole particle type in processes such as those described above.
  • the present invention involves the discovery that two problems involved in the activating particle-vibratory container processes discussed above can be solved by the use of a particular type of activating particle.
  • the extremely high volume of particles to electrolyte tends to create a serious interference with current flow between the anodes and the cathodethe particles serving to cause a plurality of tortuous, interrupted paths for such current to follow.
  • the volume of electrolyte in one instance is suificiently high to permit rapid deposition rates, throwing power is not improved. In the other instances where throwing power is improved, the electrolyte volume is so low as to limit the speed to essentially conventional rates. It would be desirable to increase the throwing power without this decrease in plating rate.
  • the activating particles By using as the activating particles a composite particle having a body or core portion formed of electrically conductive material (usually but not necessarily the same metal as is intended to be deposited) with a protective outer covering or sheath or non-conductive material which is sufiiciently hard as to permit the particle to act dynamically hard, (generally such sheath must have a Knoop hardness of about 500 or greater) where such outer sheath is perforated or open at least at one point on the surface of the particle to expose the metal or electricallyconductive underlying core portion, both of the above problems can be solved.
  • the particle cores being electrically conductive, provide reasonably direct paths for current flow and the particles themselves act as bi-polar electrodes-the side of the exposed metal toward the anode at any given instant tending to act as a cathode and having metal deposited on the core with the side towards the cathode tending to act as an anode and giving up metal ions.
  • those particles immediately adjacent the surface being plated provide a high supply of metal ions at the point necessary to afford an adequate supply for even, uniform thickness deposition even on a contoured surface.
  • FIG. 1 is a view in cross section of a typical particle of the present invention.
  • FIG. 2 is a perspective view in partial cross section of a variation in shape of a particle of the present invention.
  • FIG. 3 is a schematic illustration showing the relationship of particles of the present invention to an anode and cathode.
  • FIG. 4 is an idealized view schematically illustrating one current path through the system shown in FIG. 3 and illustrating the bi-polar effect.
  • the activating particles of the present invention are preefrably formed with a metallic core of the metal to be deposited in the system in which the particles are to be used, i.e., for a copper plating system, the particle core is copper and for a nickel plating system, the core is nickel.
  • the surrounding non-conductive sheath should preferably be of a relatively hard, impact-transmitting material, i.e., having relatively high non-energy-absorbing characteristics. Most of the thermosetting resins fall into this category as do the ceramic bonds used in and known to the art of bonded abrasives.
  • the sheath In addition to being nonenergy-absorbing and non-conductive, the sheath should possess the property of being easily wet by the electrolyte in which it is to be used and should also be resistant to chemical attack by such electrolyte.
  • the hardness of the outer sheath should generally be at least slightly harder than that of the metal to be plated but since higher hardnesses do not appear to produce adverse effects, it is preferred, in order to avoid experimentation to utilize for such sheaths materials having a hardness of about Knoop 500 or greater.
  • smooth surfaced particles are satisfactory although particles with rough surfaces are satisfactory.
  • the electrolyte in the plating zone once movement of the particles is initiated
  • micro-roughness is an essential feature of the particle surface.
  • Suitable materials for forming the particles of the present invention include, as indicated above, any conductive material which will accept a metal deposit thereon and preferably the specific metal which the particle is to be used to help deposit. These include all of the conductive metals which are capable of electrodeposition.
  • the preferred coating is a ceramic such as aluminum oxide, silicon carbide, boron carbide or the like, and again, preferably, such coating will have embedded therein or anchored thereby a plurality of very small particles of any of the conventionally-used abrasive materials such as silicon carbide, aluminum oxide, flint, emery, garnet or the like. These very small particles in the sheath will generally have an average diameter in the vicinity of 1 to 10 microns.
  • thermosetting resins resistant to the electrolyte with which the particles are to be used, may also be used to form the sheath either alone or again with the occlusion of small abrasive particles.
  • resins include phenolics, polyesters, urea-formaldehyde resins, polyethers, polyamides or the like.
  • the size of the particles in the present invention should generally be in the range of 0.01 to 0.25 inch in average maximum dimension with the preferred range being between 0.02 and 0.125 inch. Particles of varying sizes and shapes may be blended together to vary the degree of activation of the eelctrodeposit if desired.
  • the shape of the particles may vary within wide limits from extremely irregular to very uniform geometric shapes.
  • the particles are in the shape of short cylinders although as is illustrated in FIG. 2, more complex shapes are contemplated and may be particularly desirable in some instances.
  • FIG. 1 illustrates in cross section a preferred form of the particles of the present invention.
  • the particle 10 consists of an electrically-conductive metal core portion 11 and a nonconductive sheath portion 12 surrounding the core portion 11 except at the ends 13. Embedded in the sheath portion 12 are a plurality of small hard particles 14. The ends 13 of core portion 11 are dished-in so that the metal 11 does not extend out as far as the protecting nonconductive sheath portion 12. This is accomplished as is described below by etching the particles after they are formed.
  • the non-conductive sheath 12 is a ceramic coating containing small abrasive grains.
  • the particle is formed by coating a continuous small-diameter metal wire or rod with a ceramic mixture, fusing the ceramic to cause it to harden and become permanently bonded to the wire, and then severing the coated wire at short intervals to produce short coated cylinders open at each end.
  • the particles are then immersed in an etching solution, e.g. nitric acid for copper core particles, and left for approximately 1 to 2 seconds with mild agitation to cause the exposed wire cores to be etched or eaten away.
  • an etching solution e.g. nitric acid for copper core particles
  • FIG. 2 illustrates a modified version of the invention wherein the particle 20 is a doughnut shape.
  • a metal or conductive core 21 is partially encased in a sheath 22.
  • the sheath 22 is illustrated as a hard resin coating which provides incremental covering sections 22 around the outer periphery of the core 21 and additional covering sections 23, not necessarily corresponding to 22, around the inner periphery of core 21.
  • the sheathed core particle 20 has an open central portion 24 which provides more room for electrolyte movement and additionally increases the surface area of the particle 20 exposed to such electrolyte over that available with a solid particle of the same external dimensions. Portions of the core 21 are exposed between the outer sheath segments 22 as shown at 25 and. between the inner sheath segments 23 as shown at 26.
  • FIG. 3 schematically shows a portion of a plating system having a non-conforming anode 30 and a contoured cathode 31. Interposed between anode 30 and cathode 31 is a plurality of varying sized particles 32 shown here in cross section to illustrate the conductive core 33 and protective non-conductive sheath 34.
  • an electrodeposit 36 is forming on cathode 31 and, because of the bi-polar effect of these particles, such deposit 36 is relatively uniform in thickness despite the varying contours of cathode 31 upon which it is being deposited.
  • FIG. 4 schematically illustrates the function of the particle structure of the present invention.
  • a cathode 40 and anode 41 is provided in an electrolyte 42.
  • An idealized single chain of particles 43 is shown to permit clear illustration.
  • Each particle 43, as shown, has the recessed conductive core portion 44 and the surrounding non-conductive sheath 45. It is clear that current flow between the cathode 40 and anode 41 will take place from the electrode to the electrolyte, through the conductive core of a particle to the electrolyte, through the next particle core, etc., until the other electrode is reached.
  • the current flow would obviously have to be through the electrolyte only and the path of such flow would be much more indirect with consequent loss of efficiency and increase in the IR heating of the electrolyte.
  • the bi-polar effect At any given instant the particles will have a fixed orientation to one another and to the electrodes. What is shown here is a look at this particular chain of particles as they might appear at a given instant.
  • the exposed core portion 44 of each particle will act as an electrode. That portion of the core of the particle closest to anode 41 will act as a cathode and metal will deposit out thereon in such instant. Likewise, the opposite end of such core will become anodic and will tend to give off metal ions to the surrounding electrolyte.
  • Example 1 Using a diameter copper wire as the core-forming member, particles according to the present invention can be prepared by suspending 12" long sections of such wire inside diameter holes in a graphite block. The lower portion of the block is then immersed in a bath of molten alumina. A vacuum is then pulled on the holes and the molten alumina flows up and around the wire sections inside the graphite block. The block is then broken into sections between the wire segments and is burned to remove the coated wire segments. Using diamond saws, the ceramic coated wire is then cut into long pieces which may be used as is for the purposes of the present invention or preferably after a short etching with concentrated nitric acid to insure that the metal core is recessed inside the ceramic sheath. If desired, the small pieces may be pre-tumbled before using in one of the described electrodeposition processes in order to roughen the surface of the alumina.
  • Example 2 Another manner in which particles of the present invention may be prepared is exemplified by the preparation of a slurry of fine abrasive grain (Grit. 1,000 Silicon Carbide) in a thermosetting phenolic resin binder.
  • a slurry of fine abrasive grain Grit. 1,000 Silicon Carbide
  • a thermosetting phenolic resin binder e.g., phenolic resin binder.
  • the wire to be coated nickel wire is passed in continuous form through a bath of this slurry and slowly rotated in a forced hot air draft for about one hour to permit the resin to set up slightly.
  • the wire is then passed into an oven heated to about 300 F. for 2 /23 hours to cause the resin coating to cure.
  • the coated wire is cut into short segments by diamond saws, etched by a 1-3 second immersion in concentrated nitric acid, given a thorough water wash and then is ready for use in an electrodeposition process.
  • Example 3 3,500 cc. of the bi-polar activating particles of Example l (etched to recess the metal core portions) were combined with 6,000 cc. of copper sulfate plating solution (300 grams/liter CuSO -5H O and grams/liter H 50 containing 0.5% by volume of U'BAC #1'a commercially available brightener for copper). The mixture was then placed in a /3 cubic foot capacity vibratory finishing machine (Elliot Vibratub). The cathode was a steel doorknob to which a copper strike had first been applied. The doorknob was mounted in a vertical position with the knob end upwards and surrounded by four equally-spaced /2" square copper bars which acted as anodes.
  • the bars formed a hollow square with the doorknob in the center with approximately 1" distance between the cathode and each anode bar.
  • Plating was carried out with the Vibratub operating at 2,100 cycles per minute with a tub amplitude of A5".
  • a current of 50 amps. was applied which calculated out to a current density of approximately 750 amps/ft. at the cathode.
  • Plating was carried out for 2 minutes at the end of which a smooth, uniform copper plate of 1.2:.1 mils was obtained over the entire doorknob.
  • ceramic coatings can be applied by co-extrusion of the metal core with a ceramic mix or by swagging or rolling the wire in a fine grain ceramic mix followed by encasing the coated wire in a metal sheath which is dissolved or cut away after sintering the ceramic.
  • the slurry can be sprayed onto the wire or applied by coating rolls if desired.
  • Cylindrical particles can be obtained by rolling metal balls in a slurry and after the resin mixture has set up, abrading away the resin sheath on one surface of References Cited UNITED STATES PATENTS 1. In a process wherein multiple small particles are used 1,051,556 1/1913 consign?
  • the im- 5 1594509 8/1926 Rosenqulst 204 217 provernent which comprises utilizing as such small par- 3042592 7/1962 Schaer 204-.51 ticles bi-polar particles comprising a metallic core mem- R EDMUNDSON, Primary Examiner ber encapsulated 111 a surrounding non-conductive sheath having at least one opening permitting contact between US. Cl. X.R.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Electrolytic Production Of Metals (AREA)
  • Electroplating Methods And Accessories (AREA)
US147409A 1971-05-27 1971-05-27 Polar activating particles for electrodeposition process Expired - Lifetime US3699017A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5804052A (en) * 1994-05-26 1998-09-08 Atotech Deutschland Gmbh Method and device for continuous uniform electrolytic metallizing or etching

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5804052A (en) * 1994-05-26 1998-09-08 Atotech Deutschland Gmbh Method and device for continuous uniform electrolytic metallizing or etching

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DE2224392A1 (de) 1972-12-21
DE2224392C3 (de) 1975-10-09
DE2224392B2 (de) 1974-07-18
FR2139123A1 (de) 1973-01-05
FR2139123B3 (de) 1975-08-08

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