US2338321A - Method of electropolishing steel - Google Patents

Method of electropolishing steel Download PDF

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Publication number
US2338321A
US2338321A US245224A US24522438A US2338321A US 2338321 A US2338321 A US 2338321A US 245224 A US245224 A US 245224A US 24522438 A US24522438 A US 24522438A US 2338321 A US2338321 A US 2338321A
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US
United States
Prior art keywords
steel
steels
solution
polished
polishing
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US245224A
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English (en)
Inventor
Charles L Faust
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Battelle Memorial Institute Inc
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Battelle Memorial Institute Inc
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Filing date
Publication date
Priority claimed from US241975A external-priority patent/US2334699A/en
Application filed by Battelle Memorial Institute Inc filed Critical Battelle Memorial Institute Inc
Priority to US245224A priority Critical patent/US2338321A/en
Application granted granted Critical
Publication of US2338321A publication Critical patent/US2338321A/en
Priority to CH271130D priority patent/CH271130A/fr
Priority to BE478064A priority patent/BE478064A/fr
Priority to NL136944A priority patent/NL71883C/nl
Priority to LU28863A priority patent/LU28863A1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • 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

Definitions

  • This invention relates to a method of electropolishing steel and more particularly to the anodic treatment of plain carbon and low alloy steels to impart thereto a lustrous, mirror-like polish.
  • the method to which this invention pertains involves making the steel to be polished the anode in an electrolytic bath of suitable composition and passing a current of sufficient density and for a suflicient length of time through the bath to produce a high lustre or polish on the steel.
  • an electrolytic solution of the composition hereinafter described results are obtained that transcend the mere electrolytic cleaning process, in that there is produced a highly lustrous or polished surface.
  • This high lustre is an important feature of my invention and one that sharply distinguishes it from prior art finishes produced in the el ctrolytic cleaning of metals. 1
  • the electrolytic solution that I have found to possess the most general effectiveness in the polishing of steels comprises a mixture of sulfuric, phosphoric and chromic acids in such proportions that the combined acid concentration is at least 50%, and preferably over 60% by weight of the solution, the balance being mainly water. While it is possible to produce polishes with mixtures of sulfuric, phosphoric and chromic acids containing as much as 50% water, I prefer to keep the water content of the electrolytic bath relatively low, since I have found, in general, that baths containing lower proportions of water may be operated at lower current densities, and therefore at lower cost, to give satisfactory polishes. I therefore prefer to have the total acid content kept within the range of 60 to 90%, the balance being mainly water.
  • Both the sulfuric and phosphoric acid concentrations should .be in excess of 5%, with an upper limit of concentration for each of about 80%, although the upper limit is not critical and might be exceeded except for practical reasons.
  • the sulfuric acid concentration should be between and -60% and the phosphoric acid concentration between 15 and 70%.
  • chromic acid to the sulfuricphosphoric acid solution greatly increases the polishing effect toward steels, and I prefer to add chromic acid in substantial amounts up to about although as low as 0.5% chromic from 63 to 67% ortho phosphoric acid represents a narrower, preferred range for'my bath compotion.
  • the process can be operated with anode current densities varying from 50 to 1000 amperes per sq. ft., but preferably between 100 and 400 amperes per sq. it. It will be understood that even lower current densities may be employed, but longer times of treatment will be required and the process may, for that reason, be uneconomical. Higher current densities than indicated by the foregoing range may also be employed, but in that case the higher current costs offset the saving in time.
  • the length of time to effect the desired results depends upon the magnitude of the current densities employed, and to some extent upon the particular metal to be polished and the character of its surface initially. Rough surfaces, of course, require a longer time to polish than relatively smooth ones.
  • Bath composition 1 Per cent Sulfuric acid 20 Ortho phosphoric acid -5. c7 Chromic anhydrlde 2 Water 11
  • a bath of the foregoing composition produces an excellent polish on a steel containing 0.5% of molybdenum, when the steel is treated anodically therein at anode current densities of 250 amperes per sq. ft. for 30 minutes at a bath temperature of 50 C.
  • a bath of the same composition is also applicable to the electropolishing of 5% chromium steels and to copper steels containing 0.25% copper and above.
  • Bath composition My method is generally applicable to steels. but particularly to those classed as plain carbon steels and to low alloy steels having not more than 6% of combined alloy content. with such steels I am able to produce a surface which is 23, 1938, and entitled Electrolyte for the polish-.
  • Electropolished surfaces produced by my method are likewise diiierent from those made by the electrolytic treatments of the prior art.
  • the application to steels of methods heretofore used generallyv results in surfaces which are characteristically etched.
  • the crystals in the metal are strongly developed and placed in relief, so that while the surface may be bright, it is essentially a matt finish.
  • my method the development of the crystalline structure is suppressed, the surfaces of the individual crystals are levelled oil, the grain boundaries are substantially obliterated and there results a smooth and mirror-like finish.
  • the method of electro-polishing steel selected from the group consisting of plain carbon and low alloy steels, which comprises making the steel the anode in an aqueous solution of from 5 to 80% of sulfuric acid by weight of said solution, from 5 to 80% of phosphoric acid by weight of said solution and from 0.5 to 20% of chromic acid by weight of said solution, the combined acid concentration being above but not over 90% by weight of said solution, the balance being essentially water, and passing therethrough an electric current of a density between 50 and 1000 amperes per square foot.
  • the method of electro-polishing steel selected from the group consisting of plain carbon and low alloy steels, which comprises making the steel the anode in an aqueous solution of from 15 to of sulfuric acid by weight of said solution, from 15 to of phosphoric acid by weight of said solution and from 0.5 to 20% of chromic acid by weight of said solution, the combined acid concentration being above 50% but-not over by weight of said solution, the balance being essentially water, and passing therethrough an electric current of a density between 50 amperes and 1000 amperes per square foot.
  • the method of electro-polishing steel selectedfrom the group consisting of plain carbon and low alloy steels, which comprises making the steel the anode in an aqueous solution of from 15 to 20% of sulfuric acid by weight of said solution, from 63 to67% of phosphoric acid by weight of said solution and from 2 to 10% of chromic acid by weight of said solution, the balance being essentially water, and passing an electric current therethrough of sufllclent density and for a suflicient length of time to produce a polish on said steel.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • ing And Chemical Polishing (AREA)
US245224A 1938-11-23 1938-12-12 Method of electropolishing steel Expired - Lifetime US2338321A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US245224A US2338321A (en) 1938-11-23 1938-12-12 Method of electropolishing steel
CH271130D CH271130A (fr) 1938-11-23 1947-07-28 Procédé pour le polissage anodique des métaux.
BE478064A BE478064A (d) 1938-11-23 1947-12-11
NL136944A NL71883C (nl) 1938-11-23 1947-12-15 Werkwijze voor het anodisch polijsten van staal en staalalliages, nikkel en nikkelalliages, aluminium en aluminiumalliages en molybdeen
LU28863A LU28863A1 (fr) 1938-11-23 1947-12-31 Electrolyte et procédé pour le polissage anodique des métaux

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US241975A US2334699A (en) 1938-11-23 1938-11-23 Electrolyte for the polishing of metal surfaces and method of use
US245224A US2338321A (en) 1938-11-23 1938-12-12 Method of electropolishing steel

Publications (1)

Publication Number Publication Date
US2338321A true US2338321A (en) 1944-01-04

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ID=26934737

Family Applications (1)

Application Number Title Priority Date Filing Date
US245224A Expired - Lifetime US2338321A (en) 1938-11-23 1938-12-12 Method of electropolishing steel

Country Status (5)

Country Link
US (1) US2338321A (d)
BE (1) BE478064A (d)
CH (1) CH271130A (d)
LU (1) LU28863A1 (d)
NL (1) NL71883C (d)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2550544A (en) * 1947-11-14 1951-04-24 Battelle Development Corp Method of anodically polishing aluminum
US2694678A (en) * 1951-01-25 1954-11-16 Du Pont Electropolishing process and composition
US4935112A (en) * 1988-04-07 1990-06-19 Seneca Wire And Manufacturing Company Continuous steel strand electrolytic processing
US5087342A (en) * 1988-04-07 1992-02-11 Seneca Wire And Manufacturing Company Continuous steel strand electrolytic processing
US5380408A (en) * 1991-05-15 1995-01-10 Sandvik Ab Etching process
US20050045250A1 (en) * 2003-09-03 2005-03-03 Rakowski James A. Oxidation resistant ferritic stainless steels
US20060286432A1 (en) * 2005-06-15 2006-12-21 Rakowski James M Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US20060285993A1 (en) * 2005-06-15 2006-12-21 Rakowski James M Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US20060286433A1 (en) * 2005-06-15 2006-12-21 Rakowski James M Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US12043915B2 (en) 2019-10-08 2024-07-23 Lake Region Manufacturing, Inc. Electropolishing of MP35N wire for fatigue life improvement of an implantable lead

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2550544A (en) * 1947-11-14 1951-04-24 Battelle Development Corp Method of anodically polishing aluminum
US2694678A (en) * 1951-01-25 1954-11-16 Du Pont Electropolishing process and composition
US4935112A (en) * 1988-04-07 1990-06-19 Seneca Wire And Manufacturing Company Continuous steel strand electrolytic processing
US5087342A (en) * 1988-04-07 1992-02-11 Seneca Wire And Manufacturing Company Continuous steel strand electrolytic processing
US5380408A (en) * 1991-05-15 1995-01-10 Sandvik Ab Etching process
US20050045250A1 (en) * 2003-09-03 2005-03-03 Rakowski James A. Oxidation resistant ferritic stainless steels
US8518234B2 (en) * 2003-09-03 2013-08-27 Ati Properties, Inc. Oxidation resistant ferritic stainless steels
US20060286433A1 (en) * 2005-06-15 2006-12-21 Rakowski James M Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US20060285993A1 (en) * 2005-06-15 2006-12-21 Rakowski James M Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US7842434B2 (en) 2005-06-15 2010-11-30 Ati Properties, Inc. Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US7981561B2 (en) 2005-06-15 2011-07-19 Ati Properties, Inc. Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US20110229803A1 (en) * 2005-06-15 2011-09-22 Ati Properties, Inc. Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US8158057B2 (en) 2005-06-15 2012-04-17 Ati Properties, Inc. Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US8173328B2 (en) 2005-06-15 2012-05-08 Ati Properties, Inc. Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US20060286432A1 (en) * 2005-06-15 2006-12-21 Rakowski James M Interconnects for solid oxide fuel cells and ferritic stainless steels adapted for use with solid oxide fuel cells
US12043915B2 (en) 2019-10-08 2024-07-23 Lake Region Manufacturing, Inc. Electropolishing of MP35N wire for fatigue life improvement of an implantable lead

Also Published As

Publication number Publication date
BE478064A (d) 1948-01-31
LU28863A1 (fr) 1948-03-03
NL71883C (nl) 1953-03-16
CH271130A (fr) 1950-10-15

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