US2515192A - Method of electroplating - Google Patents

Method of electroplating Download PDF

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US2515192A
US2515192A US555954A US55595444A US2515192A US 2515192 A US2515192 A US 2515192A US 555954 A US555954 A US 555954A US 55595444 A US55595444 A US 55595444A US 2515192 A US2515192 A US 2515192A
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current
antimony
plating
plating bath
direct current
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Allan E Chester
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Poor and Co
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Poor and Co
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Priority to US174241A priority patent/US2606147A/en
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    • 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
    • C25D5/18Electroplating using modulated, pulsed or reversing current
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S204/00Chemistry: electrical and wave energy
    • Y10S204/08AC plus DC
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S204/00Chemistry: electrical and wave energy
    • Y10S204/09Wave forms

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  • This invention relates to a new and improved method of electroplating, and more particularly to a method of electrodepositing metals from a plating bath in a new and improved manner adapted to produce substantially uniform distribution on articles or objects of coniigurations such that the ordinary type of electroplating causes uneven distribution of the electrodeposited metal.
  • One of the objects of the present invention is to provide a new and improved method for overcoming the difficulty mentioned above and for electrodepositing metals from plating baths in a uniform manner.
  • Another object of the invention is to provide a new and improved method for electrodepositing metals on ilat sheets or other flat objects in a manner such that substantial uniformity of distribution is obtained.
  • a still further object is the provision of a new and improved method for controlling the distribution of a metal from a plating bath
  • FIG. 1 illustrates diagrammatically one form of apparatus suitable for the practice of the invention
  • Fig. 2 illustrates graphically one of the limits of the wave form of the plating current
  • Fig. 3 illustrates another limit of the wave form of the plating current in accordance with f the preferred practice of the invention.
  • the invention involves a new and improved method of controlling the distribution of metal deposited on an electrically conducting surface from a plating bath by supern imposing alternating current on direct current within certain predetermined limits.
  • the invention is especially applicable to electroplating operations in which the work or article is so shaped that the electrodeposited metal builds up in some are-as more than others.
  • the plating current for the purpose of this invention may be described as an vasymmetric alternating current in which the negative peak value of the wave 'ing time and the vertical axis amplitude. peak values are calculated from the equation to -2/3 of the positive peak value (as illustrated in Fig. 3).
  • the apparatus illustrated comprises a suitable receptacle l containing the plating bath, provided with one or more electrodes, generally indicated at 2, and a work piece or conducting surface to be plated, generally indicated at 3.
  • the electrode 2 forms the anode and the work piece 3 the cathode.
  • the anode 2 is connected by suitable conductors to the secondary 4 of a power transformer having a core 5 and a primary E.
  • the primary 6 is connected to a regulating autotransformer, generally illustrated at l, which in turn is connected to a suitable source of electrical energy, such as a 220 or 440 volt alternating current.
  • Direct current is supplied by means of a low voltage current generator, generally shown at 8, one side of which passes to the work piece 3 vthrough a rheostat 9, and the other side of which is connected to the secondary 4 in the manner shown.
  • Fig. 3 represents the maximum the purpose of this invention.
  • Any wave form ysimilar to Fig. 2 in which the negative .peak value .is positive cr above the X-axis may be described as pulsating direct current.
  • the apparatus described and the hook-up of the component parts is believed to represent a new and improved system for the electrodeposition of metals by the superimposition of an alternating current on a direct current, irrespective of whether the ratios of alternating current to direct current are within the limits preferred for uniform distribution.
  • thisk type of apparatus may be employed in plating articles of any configuration with other ratios of alternating current to direct current where the form varies from zero (as illustrated in Figrz) distribution of the electrodeposited metal is not an important factor.
  • This type of apparatus is suitable, therefore, for electroplating operations by the superimposition of alternating current on direct current in such a manner as to form a pulsating direct current.
  • the method of controlling distribution of the electrodeposited metal Kas described herein is especially suited for the formation of very thin, substantially uniform lms or coatings of a metal on an electrically conductive surface.
  • this invention is especially adapted for forming coatings of antimony on steel or cast iron objects in which the thickness of the coating is within the range f .000005 inch to .00005 inch.
  • Steel or cast iron objects, when plated with antimony in accordance with the invention to the thickness described are especially suitable for the addition of coatings of vitreous enamels, as described and claimed in my copending application Serial No. 555,953 led of even date herewith.
  • the thickness and uniformity of the plate is an important factorbecause it has been found that if the electrodeposited plate is insufficient, the desired bonding action will not occur. The same is true if the'thickness of the coating is too great.
  • this invention makes possible new and improved results in the art of enameling, as well as new and improved results in controlling the distribution of metals by electrodeposition.
  • Example I In 1 gallon of commercial 18 Be. hydrochloric acid there were dissolved 6 ounces of antimony trioxide (SbaOs) 2 ounces of arsenic trioxide (A5203) 1,/2 ounce of metallic selenium, and 3-%, based on the total weight of the mixture, of lauryl sulfate.
  • SBaOs antimony trioxide
  • A5203 arsenic trioxide
  • 3-% based on the total weight of the mixture, of lauryl sulfate.
  • the resultant mixture is an acid electrolyte or plating bath suitable for the deposition of antimony on steel or other conducting surfaces in accordance with the invention, thereby to produce a ground coat to which the vitreous enamel is applied.
  • the article to be plated e. g., an article made of a conventional type steel, is immersed in the foregoing electrolyte as the Icathode and is subjected to a superimposed plating bath, the metallic selenium is added as a reducing agent.
  • suitable reducing agents are dissociable sulphur compounds such as ferrie sulphide, poly sulphides, and other metals ofthe oxygen group of elements, such as tellurium.
  • the lauryl sulfate is employed as a surface active agent in order to enhance the smoothness fof deposit, which otherwise would be affected by ne dirt particles. Its use is not absolutely necessary but is desirable and preferable, in accordance with the practice of the invention. As will be understood. other acid stable wetting agents Example II
  • the plating bath may be the same as in Example I with the omission of the reducing agent (metallic selenium), the surface tension reducing agent (lauryl sulfate), and/or the arsenic trioxide, although the results are less desirable for some purposes.
  • Example III In the procedure described in Example I, an alkaline plating bath may be used instead of the acid bath, in which case a steel anode is employed, preferably made of cold rolled steel.
  • a typical composition for an alkaline bath is the following:
  • an arsenic plating bath may be used having the following composition: v
  • antimony, arsenic and bismuth are metals in Group V B of the Periodic Table (Websters New International Dictionary 2nd Edition Unabridged, 1941, vol. 2, page 1821) zinc and cadmium are in Group II B; copper in Group I B; tin in Group IV B; cerium and lanthanum are rare earth metals in Group UI; manganese is in Group VII A, and cobalt and nickel in Group VIII. y
  • the plating bath may be either an alkaline or an acid type, as for example, an alkaline zinccyanide bath, or an acid zinc bath, or an alkaline cyanide-cadmium plating bath, or an acid copper plating bath, or a cyanide-copper plating bath, or an alkaline tin plating bath.
  • the ratios of alternating to direct current which are preferably employed in accordance with the invention in order to obtain the desired Wave form, are about 2-4 volts (Root Mean Square) A. C.: 2.5 Volts D. C., preferably at current densities from 2 to 15 amperes per square foot. Alternating currents of different frequencies may be used, but it is preferable to employ either a 25 cycle or a 60 cycle current.
  • the plating time will vary depending upon the amount of metal which it is desired to deposit. Thus, for thicknesses of the type previously mentioned for vitreous enamel work, a plating time from 8 seconds to 11/2 minutes is sufficient.
  • the alternating and direct current voltages may be larger or smaller, provided that the ratio produces a predetermined wave form of the type previously described.
  • the direct current is 0.5 volt
  • the alternatingr current would be correspondingly reduced in accordance with the foregoing ratio.
  • the direct current is volts, the alternating current is increased in the foregoing ratio.
  • the plating current will be governed by the surface area of the article being plated, the size of the bath, power facilities and other factors which will be recognized by those skilled in the art.
  • antimony trichloride plating bath is intended to include plating baths of the type described in Example I where other metals or salts thereof are present in minor proportion as well as those in which such metals or salts are absent.
  • the invention provides a new and improved method for controlling the deposition of metals on electrically conducting surfaces. It is especially useful in applying even, uniform coatings to articles having a configuration in which, by ordinary direct current plating methods, the deposited metal tends to build up in some areas more than others. Thus, it is especially irnportant for electroplating flat surfaces when a thin plate of substantially uniform thickness is desired.
  • a method of controlling the electrodeposition of metals from a plating bath onto a work piece of a type in which such metals are normally deposited in greater concentrations in some areas of the work than in others by direct current plating comprising electrodeposting antimony on said work piece as a cathode from an antimony trichloride plating bath by a superimposed alternating-direct plating current comprising an alternating current to direct current ratio from about 2 to about 4 volts R. M. S'. alternating current having a frequency within the limits from about 25 cycles to about cycles to about 2.5 volts D. C., regardless of the specific current values, at current densities from about 2 to about 15 amperes per square foot for a period of time within the range from 8 seconds to about 11/2 minutes.

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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)
  • Electroplating And Plating Baths Therefor (AREA)
  • Electroplating Methods And Accessories (AREA)

Description

Patented July 18, 1950 METHOD OF ELECTROPLATING Allan E. Chester, Highland Park, Ill., assignor to Poor & Company, Chicago, Ill., a corporation of Delaware Application September 27, 1944, Serial No. 555,954
2 Claims.
l This invention relates to a new and improved method of electroplating, and more particularly to a method of electrodepositing metals from a plating bath in a new and improved manner adapted to produce substantially uniform distribution on articles or objects of coniigurations such that the ordinary type of electroplating causes uneven distribution of the electrodeposited metal.
It is well known that ilat objects, when electroplated in the usual way in an electroplating bath, tend to build up a higher concentration of metal near the edges than in the middle. This is true to some extent in objects of other congurations and various devices have been proposed in order to overcome this difiiculty.
One of the objects of the present invention is to provide a new and improved method for overcoming the difficulty mentioned above and for electrodepositing metals from plating baths in a uniform manner.
Another object of the invention is to provide a new and improved method for electrodepositing metals on ilat sheets or other flat objects in a manner such that substantial uniformity of distribution is obtained.
A still further object is the provision of a new and improved method for controlling the distribution of a metal from a plating bath,
Other features and advantages of the invention will appear hereinafter by reference to the following description thereof, in conjunction with the accompanying drawings in which Fig. 1 illustrates diagrammatically one form of apparatus suitable for the practice of the invention;
Fig. 2 illustrates graphically one of the limits of the wave form of the plating current; and
Fig. 3 illustrates another limit of the wave form of the plating current in accordance with f the preferred practice of the invention.
Generally stated, the invention involves a new and improved method of controlling the distribution of metal deposited on an electrically conducting surface from a plating bath by supern imposing alternating current on direct current within certain predetermined limits. The invention is especially applicable to electroplating operations in which the work or article is so shaped that the electrodeposited metal builds up in some are-as more than others. The plating current for the purpose of this invention may be described as an vasymmetric alternating current in which the negative peak value of the wave 'ing time and the vertical axis amplitude. peak values are calculated from the equation to -2/3 of the positive peak value (as illustrated in Fig. 3).
Referring to Fig. 1, the apparatus illustrated comprises a suitable receptacle l containing the plating bath, provided with one or more electrodes, generally indicated at 2, and a work piece or conducting surface to be plated, generally indicated at 3. As will be understood, the electrode 2 forms the anode and the work piece 3 the cathode.
The anode 2 is connected by suitable conductors to the secondary 4 of a power transformer having a core 5 and a primary E. The primary 6 is connected to a regulating autotransformer, generally illustrated at l, which in turn is connected to a suitable source of electrical energy, such as a 220 or 440 volt alternating current. Direct current is supplied by means of a low voltage current generator, generally shown at 8, one side of which passes to the work piece 3 vthrough a rheostat 9, and the other side of which is connected to the secondary 4 in the manner shown.
In Figs. 2 and 3 the wave form of the current is graphically illustrated in a conventional manner, the horizontal axis (X-X) represent- The where E is voltage. For the wave form to be asymmetric, the negative peak value must drop lbelow the X-axis. Thus, the Wave form of Fig. 2
becomes asymmetric when the negative peak v(Y1) falls below the X-aXis and is a diiierent Fig. 3 represents the maximum the purpose of this invention. Any wave form ysimilar to Fig. 2 in which the negative .peak value .is positive cr above the X-axis may be described as pulsating direct current.
In a broader sense, the apparatus described and the hook-up of the component parts is believed to represent a new and improved system for the electrodeposition of metals by the superimposition of an alternating current on a direct current, irrespective of whether the ratios of alternating current to direct current are within the limits preferred for uniform distribution. Thus, thisk type of apparatus may be employed in plating articles of any configuration with other ratios of alternating current to direct current where the form varies from zero (as illustrated in Figrz) distribution of the electrodeposited metal is not an important factor. This type of apparatus is suitable, therefore, for electroplating operations by the superimposition of alternating current on direct current in such a manner as to form a pulsating direct current.
The method of controlling distribution of the electrodeposited metal Kas described herein is especially suited for the formation of very thin, substantially uniform lms or coatings of a metal on an electrically conductive surface. For example, it has been found that this invention is especially adapted for forming coatings of antimony on steel or cast iron objects in which the thickness of the coating is within the range f .000005 inch to .00005 inch. Steel or cast iron objects, when plated with antimony in accordance with the invention to the thickness described, are especially suitable for the addition of coatings of vitreous enamels, as described and claimed in my copending application Serial No. 555,953 led of even date herewith. The thickness and uniformity of the plate is an important factorbecause it has been found that if the electrodeposited plate is insufficient, the desired bonding action will not occur. The same is true if the'thickness of the coating is too great. Thus,
this invention makes possible new and improved results in the art of enameling, as well as new and improved results in controlling the distribution of metals by electrodeposition.
The invention will be further illustrated but is not limited by the following examples, in which the quantities are stated in parts by weight unless otherwise indicated:
Example I In 1 gallon of commercial 18 Be. hydrochloric acid there were dissolved 6 ounces of antimony trioxide (SbaOs) 2 ounces of arsenic trioxide (A5203) 1,/2 ounce of metallic selenium, and 3-%, based on the total weight of the mixture, of lauryl sulfate.
The resultant mixture is an acid electrolyte or plating bath suitable for the deposition of antimony on steel or other conducting surfaces in accordance with the invention, thereby to produce a ground coat to which the vitreous enamel is applied. The article to be plated, e. g., an article made of a conventional type steel, is immersed in the foregoing electrolyte as the Icathode and is subjected to a superimposed plating bath, the metallic selenium is added as a reducing agent. Other examples of suitable reducing agents are dissociable sulphur compounds such as ferrie sulphide, poly sulphides, and other metals ofthe oxygen group of elements, such as tellurium.
.The lauryl sulfate is employed as a surface active agent in order to enhance the smoothness fof deposit, which otherwise would be affected by ne dirt particles. Its use is not absolutely necessary but is desirable and preferable, in accordance with the practice of the invention. As will be understood. other acid stable wetting agents Example II The plating bath may be the same as in Example I with the omission of the reducing agent (metallic selenium), the surface tension reducing agent (lauryl sulfate), and/or the arsenic trioxide, although the results are less desirable for some purposes.
Example III In the procedure described in Example I, an alkaline plating bath may be used instead of the acid bath, in which case a steel anode is employed, preferably made of cold rolled steel.
A typical composition for an alkaline bath is the following:
4.4 ounces potassium carbonate 2.11 ounces antimony sulphide (SbzSs) in one quart of water boiled for one hour and then filtered, the water lost by evaporation being replaced.
With an alkaline bath of this type the ratio of alternating current to direct current may be varied from that described in Example I in order to obtain the optimum plating conditions and to retain a wave form within the preferred range previously described, as indicated by the minimum and maximum limits of Figs. 2 and 3.`
Example IV Instead of the antimony plating bath, an arsenic plating bath may be used having the following composition: v
1% ounces sodium arsenate 0.8 ounce 98% potassium cyanide 1 quart of water.
These are boiled together for 1/2 hour, then filtered and used at a temperature of 167 to 176 F. The ratios of alternating to direct current may be varied in order to obtain the optimum wave form in the manner previously described.
It will be understood that the invention is susceptible to some variation and'modification in the manner of its practical application. Other metals than those described in the examples may be electrodeposited in accordance with the invention, including for example zinc, cadmium, tin, copper, bismuth, cerium, lanthanum, thorium, nickel, cobalt, and manganese.
As will be understood, antimony, arsenic and bismuth are metals in Group V B of the Periodic Table (Websters New International Dictionary 2nd Edition Unabridged, 1941, vol. 2, page 1821) zinc and cadmium are in Group II B; copper in Group I B; tin in Group IV B; cerium and lanthanum are rare earth metals in Group UI; manganese is in Group VII A, and cobalt and nickel in Group VIII. y
The plating bath may be either an alkaline or an acid type, as for example, an alkaline zinccyanide bath, or an acid zinc bath, or an alkaline cyanide-cadmium plating bath, or an acid copper plating bath, or a cyanide-copper plating bath, or an alkaline tin plating bath.
The ratios of alternating to direct current which are preferably employed in accordance with the invention in order to obtain the desired Wave form, are about 2-4 volts (Root Mean Square) A. C.: 2.5 Volts D. C., preferably at current densities from 2 to 15 amperes per square foot. Alternating currents of different frequencies may be used, but it is preferable to employ either a 25 cycle or a 60 cycle current. The plating time will vary depending upon the amount of metal which it is desired to deposit. Thus, for thicknesses of the type previously mentioned for vitreous enamel work, a plating time from 8 seconds to 11/2 minutes is sufficient. It will be understood that higher current densities may be used, and that the alternating and direct current voltages may be larger or smaller, provided that the ratio produces a predetermined wave form of the type previously described. Thus, if the direct current is 0.5 volt, the alternatingr current would be correspondingly reduced in accordance with the foregoing ratio. If the direct current is volts, the alternating current is increased in the foregoing ratio.
The plating current will be governed by the surface area of the article being plated, the size of the bath, power facilities and other factors which will be recognized by those skilled in the art.
The expression antimony trichloride plating bath is intended to include plating baths of the type described in Example I where other metals or salts thereof are present in minor proportion as well as those in which such metals or salts are absent.
The invention provides a new and improved method for controlling the deposition of metals on electrically conducting surfaces. It is especially useful in applying even, uniform coatings to articles having a configuration in which, by ordinary direct current plating methods, the deposited metal tends to build up in some areas more than others. Thus, it is especially irnportant for electroplating flat surfaces when a thin plate of substantially uniform thickness is desired.
The invention is hereby claimed as follows:
1. In a method of controlling the electrodeposition of antimony from an antimony trichloride plating bath onto an electrically conducting object of a type in which the antimony would normally be deposited in greater concentrations in some areas than in others by a direct plating current; the step which comprises electrodepositing the antimony from an antimony trichloride plating bath by subjecting said object as a cathode in the plating bath to a plating current having an asymmetric alternating Wave form comprising an alternating current superimposed on a direct current in the ratio of 2-4 volts R. M. S. to 2.5 volts D. C., regardless of the specic current values, at current densities from about 2 to about 15 amperes per square foot.
2. In a method of controlling the electrodeposition of metals from a plating bath onto a work piece of a type in which such metals are normally deposited in greater concentrations in some areas of the work than in others by direct current plating; the step which comprises electrodeposting antimony on said work piece as a cathode from an antimony trichloride plating bath by a superimposed alternating-direct plating current comprising an alternating current to direct current ratio from about 2 to about 4 volts R. M. S'. alternating current having a frequency within the limits from about 25 cycles to about cycles to about 2.5 volts D. C., regardless of the specific current values, at current densities from about 2 to about 15 amperes per square foot for a period of time within the range from 8 seconds to about 11/2 minutes.
ALLAN E. CHESTER.
REFERENCES CITED The following references are of record in the le of this patent:
UNITED STATES PATENTS Niunber Name Date 792,307 Betts June 13, 1905 1,918,605 Jones July 18, 1933 2,063,760 Schulein Dec. 8, 1936 2,401,738 Diffenderfer June 1l, 1946 p 2,443,599 Chester i June 22, 1948 OTHER REFERENCES Transactions of Faraday Society, vol. 24 (1928), pp. 348-358; vol. 18 (1922), pp. 102-111.
American Electroplaters Society Monthly Review, Feb. 1944, p. 168.
Transactions of American Electrochemical Society, vol. 41 1922), pp. 151-180.

Claims (1)

1. IN A METHOD OF CONTROLLING THE ELECTRODEPOSITION OF ANTIMONY FROM AN ANTIMONY TRICHLORIDE PLATING BATH ONTO AN ELECTRICALLY CONDUCTING OBJECT OF A TYPE IN WHICH THE ANTIMONY WOULD NORMALLY BE DEPOSITED IN GREATER CONCENTRATIONS IN SOME AREAS THAN IN OTHERS BY A DIRECT PLATING CURRENT; THE STEP WHICH COMPRISES ELECTRODEPOSITING THE ANTIMONY FROM AN ANTIMONY TRICHLORIDE PLATING BATH BY SUBJECTING SAID OBJECT AS A CATHODE IN THE PLATING BATH TO A PLATING CURRENT HAVING AN ASYMMETRIC ALTERNATING WAVE FORM COMPRISING AN ALTERNATING CURRENT SUPERIMPOSED ON A DIRECT CURRENT IN THE RATIO OF 2-4 VOLTS R. M. S. TO 2.5 VOLTS D. C., REGARDLESS OF THE SPECIFIC CURRENT VALUES, AT CURRENT DENSITIES FROM ABOUT 2 TO ABOUT 15 AMPERES PER SQUARE FOOT.
US555954A 1944-09-27 1944-09-27 Method of electroplating Expired - Lifetime US2515192A (en)

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US555954A US2515192A (en) 1944-09-27 1944-09-27 Method of electroplating
GB18971/45A GB599707A (en) 1944-09-27 1945-07-24 Method of electroplating
FR912699D FR912699A (en) 1944-09-27 1945-07-24 Process for the deposition of metals by electrolytic or galvanic means
US174241A US2606147A (en) 1944-09-27 1950-07-17 Electrodeposition of arsenic

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Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2606147A (en) * 1944-09-27 1952-08-05 Poor & Co Electrodeposition of arsenic
US2619454A (en) * 1945-08-30 1952-11-25 Brush Dev Co Method of manufacturing a magnetic recording medium by electrodeposition
US2651610A (en) * 1950-07-17 1953-09-08 Poor & Co Method of electroplating zinc
US2651609A (en) * 1950-07-17 1953-09-08 Poor & Co Method of electroplating copper
US2685053A (en) * 1950-06-03 1954-07-27 Samuel D Warren Electrolytic capacitor system
US2706170A (en) * 1951-11-15 1955-04-12 Sperry Corp Electroforming low stress nickel
US2741586A (en) * 1953-01-12 1956-04-10 North American Aviation Inc Electroplating metals
US2753299A (en) * 1953-04-23 1956-07-03 Bell Telephone Labor Inc Electroplating with antimony
US2821505A (en) * 1954-04-01 1958-01-28 John G Beach Process of coating metals with bismuth or bismuth-base alloys
US2935454A (en) * 1953-05-01 1960-05-03 Tokumoto Shin-Ichi Method of the electrodeposition of titanium metal
US3223603A (en) * 1960-04-04 1965-12-14 Inoue Kiyoshi Machining by combined spark discharge and electrolytic action
US3407125A (en) * 1965-01-18 1968-10-22 Corning Glass Works Method of making filamentary metal structures
US3417008A (en) * 1965-01-15 1968-12-17 Udylite Corp Switch for electrochemical processes
US3480522A (en) * 1966-08-18 1969-11-25 Ibm Method of making magnetic thin film device
US3716464A (en) * 1969-12-30 1973-02-13 Ibm Method for electrodepositing of alloy film of a given composition from a given solution

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US792307A (en) * 1904-05-20 1905-06-13 Anson Gardner Betts Process of electrodepositing antimony.
US1918605A (en) * 1928-01-09 1933-07-18 Parker Rust Proof Co Chromium plating
US2063760A (en) * 1931-09-10 1936-12-08 Schulein Joseph Bath for and process of electrodeposition of metal
US2401738A (en) * 1943-01-01 1946-06-11 Rca Corp Phototube and method of manufacture
US2443599A (en) * 1942-05-04 1948-06-22 Poor & Co Electroplating method employing pulsating current of adjustable wave form

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US792307A (en) * 1904-05-20 1905-06-13 Anson Gardner Betts Process of electrodepositing antimony.
US1918605A (en) * 1928-01-09 1933-07-18 Parker Rust Proof Co Chromium plating
US2063760A (en) * 1931-09-10 1936-12-08 Schulein Joseph Bath for and process of electrodeposition of metal
US2443599A (en) * 1942-05-04 1948-06-22 Poor & Co Electroplating method employing pulsating current of adjustable wave form
US2401738A (en) * 1943-01-01 1946-06-11 Rca Corp Phototube and method of manufacture

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2606147A (en) * 1944-09-27 1952-08-05 Poor & Co Electrodeposition of arsenic
US2619454A (en) * 1945-08-30 1952-11-25 Brush Dev Co Method of manufacturing a magnetic recording medium by electrodeposition
US2685053A (en) * 1950-06-03 1954-07-27 Samuel D Warren Electrolytic capacitor system
US2651610A (en) * 1950-07-17 1953-09-08 Poor & Co Method of electroplating zinc
US2651609A (en) * 1950-07-17 1953-09-08 Poor & Co Method of electroplating copper
US2706170A (en) * 1951-11-15 1955-04-12 Sperry Corp Electroforming low stress nickel
US2741586A (en) * 1953-01-12 1956-04-10 North American Aviation Inc Electroplating metals
US2753299A (en) * 1953-04-23 1956-07-03 Bell Telephone Labor Inc Electroplating with antimony
US2935454A (en) * 1953-05-01 1960-05-03 Tokumoto Shin-Ichi Method of the electrodeposition of titanium metal
US2821505A (en) * 1954-04-01 1958-01-28 John G Beach Process of coating metals with bismuth or bismuth-base alloys
US3223603A (en) * 1960-04-04 1965-12-14 Inoue Kiyoshi Machining by combined spark discharge and electrolytic action
US3417008A (en) * 1965-01-15 1968-12-17 Udylite Corp Switch for electrochemical processes
US3407125A (en) * 1965-01-18 1968-10-22 Corning Glass Works Method of making filamentary metal structures
US3480522A (en) * 1966-08-18 1969-11-25 Ibm Method of making magnetic thin film device
US3716464A (en) * 1969-12-30 1973-02-13 Ibm Method for electrodepositing of alloy film of a given composition from a given solution

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Publication number Publication date
FR912699A (en) 1946-08-16
GB599707A (en) 1948-03-18

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