US3230160A - Electrolyte for electrochemical material removal - Google Patents

Electrolyte for electrochemical material removal Download PDF

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Publication number
US3230160A
US3230160A US224834A US22483462A US3230160A US 3230160 A US3230160 A US 3230160A US 224834 A US224834 A US 224834A US 22483462 A US22483462 A US 22483462A US 3230160 A US3230160 A US 3230160A
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US
United States
Prior art keywords
electrolyte
sodium nitrite
water
per liter
sodium
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
US224834A
Other languages
English (en)
Inventor
George C Kennedy
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.)
General Electric Co
Original Assignee
General Electric Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by General Electric Co filed Critical General Electric Co
Priority to US224834A priority Critical patent/US3230160A/en
Priority to CH862663A priority patent/CH428369A/de
Priority to FR942765A priority patent/FR1367099A/fr
Priority to DEG38611A priority patent/DE1258232B/de
Priority to GB36531/63A priority patent/GB985158A/en
Application granted granted Critical
Publication of US3230160A publication Critical patent/US3230160A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23HWORKING OF METAL BY THE ACTION OF A HIGH CONCENTRATION OF ELECTRIC CURRENT ON A WORKPIECE USING AN ELECTRODE WHICH TAKES THE PLACE OF A TOOL; SUCH WORKING COMBINED WITH OTHER FORMS OF WORKING OF METAL
    • B23H3/00Electrochemical machining, i.e. removing metal by passing current between an electrode and a workpiece in the presence of an electrolyte
    • B23H3/08Working media
    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25FPROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
    • C25F3/00Electrolytic etching or polishing
    • C25F3/02Etching

Definitions

  • electrolyte which conducts current between the two electrodes allowing material to be eroded electrochemically from the workpiece.
  • electrolytes In order to provide adequate conductivity in electrolytes, thus to lower the resistance to flow of current between the electrodes, a variety of salts, acids and the like are used.
  • electrolytes are highly corrosive to equipment, or produce intergranular attack on material of the workpiece. This is particularly true when the electrolyte conductivity is adjusted to provide optimum feed rates for the tool and workpiece one toward the other in order to achieve maximum material removal rates.
  • Another object is to provide an electrolyte which can be inexpensively and easily prepared, which does not become rancid and which is safe with regard to the health of workmen.
  • the electrolyte of the present invention consists essentially of an aqueous solution of 90240 grams of sodium formate and about 20-80 grams of sodium nitrite per liter of water.
  • the most effective and preferred form of the invention consists essentially of about 120 grams of sodium formate and about 26 grams of sodium nitrite per liter of water.
  • the sodium formate provides the principal amount of electrical conductivity while the sodium nitrite provides principally corrosion resistance.
  • both are salts which will ionize in water so that both will contribute some conductivity to the electrolyte.
  • the solutions resistivity decreases from about 20 ohms at about Patented Jan. 18, 1966 50 grams per liter to about 9 ohms at 400 grams per liter.
  • the resistivity further decreases so that at 50 grams per liter of sodium formate and about 175 grams per liter of sodium nitrite, the specific resistivity of an aqueous solution is between 7 and 7.5 ohms. This same condition exists up to a concentration of about 300 grams per liter of sodium formate with the same amount of sodium nitrite.
  • the specific resistivity of the solution progressively decreases until at about 400 grams per liter of sodium nitrite the specific resistivity is between 5 and 5.5.
  • a chart of aqueous solutions of the two salts sodium formate and sodium nitrite show specific resistivity areas which might appear more favorable than that of the present invention.
  • the particular composition of 120-240 grams of sodium formate and 2570 grams of sodium nitrite per liter of water unexpectedly provides an electrolyte having an overall balance of (1) relatively low specific resistivity, (2) resistance to corrosion of equipment and (3) resistance to intergranular attack on workpiece material.
  • the conductivity of aqueous electrolyte solutions including less than about grams of sodium formate and sodium nitrite up to about 80 grams per liter of water have excessively high specific resistivity. Therefore it is less desirable and less practical an electrolyte.
  • Example 1 The data of the following Table I is typical of a wide variety of solutions studied in connection with the present invention. As shown :by Examples 1, 2 and 3, the range of 2570 grams of sodium nitrite and -240 grams of sodium formate per liter of water is specifically preferred with regard to pitting of the specimen. Examples 4 and 5 show that sodium nitrite alone or in the presence of too much sodium formate will not prevent pitting of the specimen. In addition, Example 6 shows that a large amount of sodium nitrite can do more harm from a pitting corrosion point of view than can the relatively large amount of sodium formate in Example 5.
  • Example NaNOz (5/ HCOONa Specimen (al Condition) The most desirable amount of sodium formate in the electrolyte of the present invention is at about 1 pound per gallon of water (about 120 grams per liter of Water) in the presence of a particular amount of sodium nitrite.
  • the data of Table II shows that with such an amount of sodium formate, less than about 20 grams per liter of sodium nitrite will result in a large amount of corrosion, with about 20 grams per liter representing a point at which only slight corrosion of the specimen takes place. It was found that between about 25 and 80 grams of sodium nitrite per liter of Water in such a solution did not corrode the specimen Whereas about 80 grams per liter resulted in the specimens surface being pitted.
  • an unusual combination of resistance to surface corrosion and resistance to intergranular attack, along with proper conductivity, can be achieved in an electrolyte within the range of the present invention.
  • an electrolyte consisting essentially of, 25-70 grams of sodium nitrite and 120-240 grams of sodium formate per liter of water. From an economical and health point of view along with optimum material removal rates, it has been found that an electrolyte including about 25 grams of sodium nitrite and about 120 grams of sodium formate for each liter of water is particularly desirable.
  • An aqueous solution suitable for use as an electrolyte in electrochemical material removal, consisting of sodium formate, sodium nitrite and water, the sodium formate content being -240 grams per liter of water and the sodium nitrite content being 20-80 grams per liter of water.
  • An aqueous solution suitable for use as an electrolyte in electrochemical material removal, consisting of sodium formate, sodium nitrite and water, the sodium formate content being -240 grams per liter of water and the sodium nitrite content being 25-70 grams per liter of water.
  • An aqueous solution suitable for use as an electrolyte in electrochemical material removal, consisting of sodium formate, sodium nitrite and water, the sodium formate content being about 120 grams per liter of water and the sodium nitrite content being about 25 grams per liter of water.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Internal Circuitry In Semiconductor Integrated Circuit Devices (AREA)
  • Electrical Discharge Machining, Electrochemical Machining, And Combined Machining (AREA)
  • Preventing Corrosion Or Incrustation Of Metals (AREA)
US224834A 1962-09-19 1962-09-19 Electrolyte for electrochemical material removal Expired - Lifetime US3230160A (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US224834A US3230160A (en) 1962-09-19 1962-09-19 Electrolyte for electrochemical material removal
CH862663A CH428369A (de) 1962-09-19 1963-07-10 Elektrolyt
FR942765A FR1367099A (fr) 1962-09-19 1963-07-26 électrolyte
DEG38611A DE1258232B (de) 1962-09-19 1963-09-05 Elektrolyt fuer die elektrolytische Metallabtragung
GB36531/63A GB985158A (en) 1962-09-19 1963-09-17 Electrolyte for electro-chemical removal of materials

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US224834A US3230160A (en) 1962-09-19 1962-09-19 Electrolyte for electrochemical material removal

Publications (1)

Publication Number Publication Date
US3230160A true US3230160A (en) 1966-01-18

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
US224834A Expired - Lifetime US3230160A (en) 1962-09-19 1962-09-19 Electrolyte for electrochemical material removal

Country Status (4)

Country Link
US (1) US3230160A (de)
CH (1) CH428369A (de)
DE (1) DE1258232B (de)
GB (1) GB985158A (de)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4363708A (en) * 1980-05-24 1982-12-14 Daimler-Benz Aktiengesellschaft Process for exposing silicon crystals on the surface of a component of an aluminum alloy of high silicon content
US5911864A (en) * 1996-11-08 1999-06-15 Northrop Grumman Corporation Method of fabricating a semiconductor structure
US11775079B2 (en) 2020-03-26 2023-10-03 Snap Inc. Navigating through augmented reality content

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2939825A (en) * 1956-04-09 1960-06-07 Cleveland Twist Drill Co Sharpening, shaping and finishing of electrically conductive materials
US3004910A (en) * 1952-09-18 1961-10-17 George F Keeleric Apparatus for electrolytic cutting, shaping and grinding
US3046206A (en) * 1955-02-23 1962-07-24 Richard C Johnson Electro-chemical machining system

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE748265C (de) * 1941-01-22 1944-10-31 Dr Phil Adolf Robert Kroener Elektrolytisches AEtzverfahren

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3004910A (en) * 1952-09-18 1961-10-17 George F Keeleric Apparatus for electrolytic cutting, shaping and grinding
US3046206A (en) * 1955-02-23 1962-07-24 Richard C Johnson Electro-chemical machining system
US2939825A (en) * 1956-04-09 1960-06-07 Cleveland Twist Drill Co Sharpening, shaping and finishing of electrically conductive materials

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4363708A (en) * 1980-05-24 1982-12-14 Daimler-Benz Aktiengesellschaft Process for exposing silicon crystals on the surface of a component of an aluminum alloy of high silicon content
US5911864A (en) * 1996-11-08 1999-06-15 Northrop Grumman Corporation Method of fabricating a semiconductor structure
US11775079B2 (en) 2020-03-26 2023-10-03 Snap Inc. Navigating through augmented reality content

Also Published As

Publication number Publication date
GB985158A (en) 1965-03-03
DE1258232B (de) 1968-01-04
CH428369A (de) 1967-01-15

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