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US3033769A - Electropolishing refractory metals - Google Patents

Electropolishing refractory metals Download PDF

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Publication number
US3033769A
US3033769A US861450A US86145059A US3033769A US 3033769 A US3033769 A US 3033769A US 861450 A US861450 A US 861450A US 86145059 A US86145059 A US 86145059A US 3033769 A US3033769 A US 3033769A
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Prior art keywords
electropolishing
acid
columbium
percent
hydrofluoric acid
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US861450A
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Cortes Francis Richard
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Universal Cyclops Steel Corp
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Universal Cyclops Steel Corp
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Priority to US861450A priority Critical patent/US3033769A/en
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25FPROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
    • C25F3/00Electrolytic etching or polishing
    • C25F3/16Polishing
    • C25F3/22Polishing of heavy metals
    • C25F3/26Polishing of heavy metals of refractory metals

Definitions

  • This invention relates to the electropolishing of the refractory metals, especially columbium, though it is also applicable to tantalum, tungsten and molybdenum.
  • the total acid concentration in the electrolytic solution of the invention ranges from a minimum, on a volume basis, of 3.75 percent with a minimum sulfuric to hydrofluoric acid ratio of 2:1, to a maximum of approximately 7.5 percent with a maximum sulfuric acid to hydrofluoric acid ratio of 12:1, with the balance being methanol. It is to be noted that the range of acid concentrations specified is necessary to secure satisfactory results, though the actual acids used can be of a difierent concentration from that stated, for equivalent quantity-concentration combinations can be used if desired.
  • Electropolishing is accomplished in accordance with the invention while using current densities within the range of 25 to 60 amperes per square inch and using from 50 to 90 volts across the cell. Within these ranges the higher current densities and voltages are used with shorter times and conversely the lower current densities and voltages with longer times.
  • An electrolyte solution composed of 5 volume percent of sulfuric acid (.184 specific gravity), 0.4 volume percent of hydrofluoric acid (1.2 specific gravity), and the remainder methanol was prepared by adding the acids to a container that had the methanol in it.
  • the electrolytic solutions of this invention are relatively weak acid solutions compared to those shown in prior art. This is advantageous because my electrolyte is relatively non-corrosive, is safe to handle and considerably less expensive than the more concentrated solutions.
  • the solution concentration is also truly surprising when one compares the operating times (a few seconds) of my process with those of the prior art (many minutes). It is further surprising when it is observed that there was no known solution, prior to the present invention, for electropolishing columbium. It may have been thought that a very concentrated acid would be essential for treating columbium; but my discovery is directly opposed to that conclusion.
  • cathode materials can be used such, for example, as carbon or other material.
  • they in preparing surfaces for electropolishing, they must first be mechanically polished through the 3/0 metallographic paper. Polishing through the 4/0 paper or further can also be used where the condition of the specimen warrants it.
  • the method of electropolishing a refractory metal selected from the group consisting of columbium, tantalum, molybdenum and tungsten including the steps of making said refractory metal the anode in an electrolytic solution consisting essentially of hydrofluoric acid, sulfuric acid and methanol wherein the total acid concentration in said solution ranges, on a volume basis, from a minimum of 3.75 percent with a minimum sulfuric acid to hydrofluoric acid ratio of 2 to 1 to a maximum of about 7.5 percent with a maximum ratio of sulfuric acid to hydrofluoric acid of 12 to 1.
  • the method of electropolishing columbium including the step of making a part composed of columbium the anode in an electrolytic solution consisting essential- 1y of 0.1 to 3 volume percent of 1.2 specific gravity hydrofluoric acid, 2.5 to 7 volume percent of 1.84 specific gravity sulfuric acid and the remainder methanol, with the acids being used in ratios to provide a total acid concentration Within the range of about 3.75 percent to 7.5 volume percent.

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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)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)

Description

United States Patent f 3,033,769 ELECTROPOLISHHN G REFRACTORY NETALS Francis Richard Cortes, Pittsburgh, Pa., assignor to Universal-Cyclops Steel Corporation, Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. Filed Dec. 23, 1959, Ser. No. 861,450 6 Claims. (Cl. 204140.5)
This invention relates to the electropolishing of the refractory metals, especially columbium, though it is also applicable to tantalum, tungsten and molybdenum.
It is a primary object of the present invention to provide a method, and an electrolytic solution that can be used therewith, to electropolish the refractory metals in a manner particularly satisfactory for metallographic work, which method is easy to perform; effectively electropolishes in a matter of seconds; and that utilizes an electrolyte that is safe to handle and relatively inexpensive.
This and other objects are attained in accordance with my invention in which a solution composed of from 0.1 to 3 volume percent of 1.2 specific gravity (aqueous) hydrofluoric acid, and 2.5 to 7 volume percent of 1.84 specific gravity (aqueous) sulfuric acid and methanol is used under conditions hereinafter specified to electropolish columbium and the other refractory metals. By my method and electrolyte, I am able to eliectively electropolish the refractory metals very rapidly, i.e., within about to 30 seconds, and produce a surface that is fully satisfactory for purposes of metallographic work.
The total acid concentration in the electrolytic solution of the invention ranges from a minimum, on a volume basis, of 3.75 percent with a minimum sulfuric to hydrofluoric acid ratio of 2:1, to a maximum of approximately 7.5 percent with a maximum sulfuric acid to hydrofluoric acid ratio of 12:1, with the balance being methanol. It is to be noted that the range of acid concentrations specified is necessary to secure satisfactory results, though the actual acids used can be of a difierent concentration from that stated, for equivalent quantity-concentration combinations can be used if desired.
Electropolishing is accomplished in accordance with the invention while using current densities within the range of 25 to 60 amperes per square inch and using from 50 to 90 volts across the cell. Within these ranges the higher current densities and voltages are used with shorter times and conversely the lower current densities and voltages with longer times.
In operation, it has been found essential to maintain the electrolytic solution at room temperature or below, i.e., not exceeding about 70 F., to prevent the formation of an anodic film. This temperature can readily be maintained by using a full flowing electrolyte, which serves to carry away heat from the work surface. Also, conventional cooling means externally of the cell can be used, if desired, to be sure that the requisite low electrolyte temperature is maintained.
The inventign will be readily understood upon considering the following example in which the details are given by way of illustration and not by way of limitation.
An electrolyte solution composed of 5 volume percent of sulfuric acid (.184 specific gravity), 0.4 volume percent of hydrofluoric acid (1.2 specific gravity), and the remainder methanol was prepared by adding the acids to a container that had the methanol in it. A strip of columbium, prepared by mechanically polishing its surface through 3/0 metallographic paper, was made the anode in a commercially available polishing cell comprising a D.C. source of current and a stainless steel cathode. The current was then adjusted to provide a current density of 35 amperes per square inch of the columbium strip at 55 volts. After 15 seconds of operation, the power was turned off and the columbium strip was examined. The
3,033,769 Patented May 8, 1962 surface was found to be essentially bright and smooth, there being no evidence of pitting or coarseness at magnifications as low as x.
Similar results in very short times have been obtained on tantalum strip, tungsten bar stock and as-cast specimens of molybdenum. Through experience, the following ranges of electrolyte composition, current density, voltages and time of treatment have been determined to constitute the preferred ranges for the respective refractory metals indicated.
It is particularly noteworthy that the electrolytic solutions of this invention are relatively weak acid solutions compared to those shown in prior art. This is advantageous because my electrolyte is relatively non-corrosive, is safe to handle and considerably less expensive than the more concentrated solutions. The solution concentration is also truly surprising when one compares the operating times (a few seconds) of my process with those of the prior art (many minutes). It is further surprising when it is observed that there was no known solution, prior to the present invention, for electropolishing columbium. It may have been thought that a very concentrated acid would be essential for treating columbium; but my discovery is directly opposed to that conclusion.
From the foregoing data and discussion, it is evident that the present invention provides a ready solution to the problem of electropolishing the refractory metals. Electropolishing procedures for molybdenum, tantalum and tungsten have been proposed heretofore, but experience with them has demonstrated their unsuitability as measured by surface inspection under low magnification. While my invention is primarily directed to providing the art with a procedure for electropolishing columbium, it is also eflective for the other named refractory metals with the advantages already stated.
It will be appreciated by those skilled in the art that variations from the details given can be made. Other cathode materials can be used such, for example, as carbon or other material. Further, in preparing surfaces for electropolishing, they must first be mechanically polished through the 3/0 metallographic paper. Polishing through the 4/0 paper or further can also be used where the condition of the specimen warrants it.
In accordance with the provisions of the patent statutes, I have described my invention and set forth what is now believed to represent its best embodiment. However, I desire to have it understood that, within the scope of the appended claims, the invention can be practiced otherwise than as specifically described.
I claim:
1. The method of electropolishing a refractory metal selected from the group consisting of columbium, tantalum, molybdenum and tungsten including the steps of making said refractory metal the anode in an electrolytic solution consisting essentially of hydrofluoric acid, sulfuric acid and methanol wherein the total acid concentration in said solution ranges, on a volume basis, from a minimum of 3.75 percent with a minimum sulfuric acid to hydrofluoric acid ratio of 2 to 1 to a maximum of about 7.5 percent with a maximum ratio of sulfuric acid to hydrofluoric acid of 12 to 1.
2. The method of electropolishing columbium including the step of making a part composed of columbium the anode in an electrolytic solution consisting essential- 1y of 0.1 to 3 volume percent of 1.2 specific gravity hydrofluoric acid, 2.5 to 7 volume percent of 1.84 specific gravity sulfuric acid and the remainder methanol, with the acids being used in ratios to provide a total acid concentration Within the range of about 3.75 percent to 7.5 volume percent.
3. A method according to claim 2 in which said columbium is in the form of a strip and current is passed through said electrolytic solution to provide a current density at saidistrip of about 30 to 35 amperes per square inch.
4. A method in accordance with claim 1 in which said refractory metal is tantalum and it is subjected to current for a period of time of about 8 to 25 seconds at a current ends at a current density of about 35 to 45 amperes per square inch.
6. A method in accordance with claim 1 in which said refractory metal part is tungsten bar, and current is passed through said electrolyte for about 8 to 15 seconds at a current density on the order of 30 amperes per square inch.
References Cited in the file of this patent UNITED STATES PATENTS 2,443,651 Cannizzaro June 22, 1948 2,461,035 Clingan Feb. 8, 1949 2,466,095 Gall et al. Apr. 5, 1949 2,674,571 Prosen Apr. 6, 1954 2,740,755 Couch et a1. Apr. 6, 1954 2,953,507 Palrne Sept. 20, 1960 FOREIGN PATENTS 536,710 Canada Feb. 5, 1957 OTHER REFERENCES Metals Handbook, published by the American Society for Metals, 1948, page 1137.

Claims (1)

1. THE METHOD OF ELECTROPOLISHING A REFRACTORY METAL SELECTED FROM THE GROUP CONSISTING OF COLUMBIUM, TANTALUM, MOLYBDENUM AND TUNSTEN INCLUDING THE STEPS OF MAKING SAID REFRACTORY METAL THE ANODE IN AN ELECTROLYTIC SOLUTION CONSISTING ESSENTIALLY OF HYDROFLUORIC ACID, SUL FURIC ACID AND METHANOL WHEREIN THE TOTAL ACID CONCENTRSTION IN SAID SOLUTION RANGES, ON A VOLUME BASIS, FROM A MINIMUM OF 3.75 PERCENT WITH A MINIMUM SULFURIC ACID TO HYDROFLUORIC ACID RATIO OF 2 TO 1 TO A MAXIMUM OF ABOUT 7.5 PERCENT WITH A MAXIMUM RATIO OF SULFURIC ACID TO HYDROFLUORIC ACID OF 12 TO 1.
US861450A 1959-12-23 1959-12-23 Electropolishing refractory metals Expired - Lifetime US3033769A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4169027A (en) * 1977-07-05 1979-09-25 Kernforschungsanlage Julich Gesellschaft Mit Beschrankter Haftung Method of electrochemically processing the surface of a workpiece of molybdenum or of an alloy containing a high proportion of molybdenum
US20120000793A1 (en) * 2002-11-25 2012-01-05 Hong Wang Electrochemical removal of tantalum-containing materials

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2443651A (en) * 1944-12-05 1948-06-22 Westinghouse Electric Corp Process of electroplating on tungsten
US2461035A (en) * 1944-02-23 1949-02-08 Armco Steel Corp Electrolytic stainless steel polishing
US2466095A (en) * 1944-03-15 1949-04-05 Pennsylvania Salt Mfg Co Electrochemical process for polishing tantalum
US2674571A (en) * 1951-07-06 1954-04-06 Nobilium Proc Inc Method of electropolishing dental appliances
US2740755A (en) * 1953-04-01 1956-04-03 Dwight E Couch Electropolishing with phosphorous acid
CA536710A (en) * 1957-02-05 Armco Steel Corporation Polishing stainless steel
US2953507A (en) * 1952-10-09 1960-09-20 Schwarzkopf Dev Co Method for electrolytic thickness reduction of metal wires

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA536710A (en) * 1957-02-05 Armco Steel Corporation Polishing stainless steel
US2461035A (en) * 1944-02-23 1949-02-08 Armco Steel Corp Electrolytic stainless steel polishing
US2466095A (en) * 1944-03-15 1949-04-05 Pennsylvania Salt Mfg Co Electrochemical process for polishing tantalum
US2443651A (en) * 1944-12-05 1948-06-22 Westinghouse Electric Corp Process of electroplating on tungsten
US2674571A (en) * 1951-07-06 1954-04-06 Nobilium Proc Inc Method of electropolishing dental appliances
US2953507A (en) * 1952-10-09 1960-09-20 Schwarzkopf Dev Co Method for electrolytic thickness reduction of metal wires
US2740755A (en) * 1953-04-01 1956-04-03 Dwight E Couch Electropolishing with phosphorous acid

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4169027A (en) * 1977-07-05 1979-09-25 Kernforschungsanlage Julich Gesellschaft Mit Beschrankter Haftung Method of electrochemically processing the surface of a workpiece of molybdenum or of an alloy containing a high proportion of molybdenum
US20120000793A1 (en) * 2002-11-25 2012-01-05 Hong Wang Electrochemical removal of tantalum-containing materials
US9068273B2 (en) * 2002-11-25 2015-06-30 Quantum Global Technologies LLC Electrochemical removal of tantalum-containing materials

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