US2067703A - Electrolytic device - Google Patents

Electrolytic device Download PDF

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Publication number
US2067703A
US2067703A US526118A US52611831A US2067703A US 2067703 A US2067703 A US 2067703A US 526118 A US526118 A US 526118A US 52611831 A US52611831 A US 52611831A US 2067703 A US2067703 A US 2067703A
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Prior art keywords
aluminum
electrode
electrodes
film
cleaning
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Expired - Lifetime
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US526118A
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Robinson Preston
Joseph L Collins
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SPRAGUE SPECIALTIES CO
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SPRAGUE SPECIALTIES CO
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Publication date
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Priority to US526118A priority Critical patent/US2067703A/en
Priority to US1432A priority patent/US2035022A/en
Application granted granted Critical
Publication of US2067703A publication Critical patent/US2067703A/en
Anticipated expiration legal-status Critical
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Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01GCAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES OR LIGHT-SENSITIVE DEVICES, OF THE ELECTROLYTIC TYPE
    • H01G9/00Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
    • H01G9/0029Processes of manufacture

Definitions

  • Such films consist of partially hydrated aluminum oxide and have a uni-directional character.
  • the oxide layer which forms on aluminum when exposed to the action of acids or to air, While chemically similar to the substance of the film built up in the electrolytic forming process, substantially differs therefrom in its insulating and dielectric properties.
  • the electrodes are preferably subjected to rinsing.
  • This oxide layer is not removed film formed in an acidic cleaner.
  • the capacity of the condenser using the first electrode was 6.2 MFD and its power factor 24%, while of the condenser using the second electrode, the capacity was 7.1 MFD and the power factor 15%.
  • the electrodes instead of being subjected to a preliminary chemical cleaning, undergo a preliminary forming process, which consists of placing the electrodes in a slightly acidic electrolyte, for instance, borax and boric acid in which the electrodes are subjected to a short formation.
  • a preliminary forming process which consists of placing the electrodes in a slightly acidic electrolyte, for instance, borax and boric acid in which the electrodes are subjected to a short formation.
  • a thin oxide film covers the electrode, which film also includes the surface contaminations of the aluminum.
  • the electrodes are submerged in an alkaline solution, for instance, borax, sodium phosphate, etc., which attacks and removes the preliminary film without oxidizing or attacking the aluminum. Thereafter, the electrodes are subjected to the regular forming process, preferably in a slightly acidic electrolyte.
  • an alkaline solution for instance, borax, sodium phosphate, etc.
  • the alkaline solution only dissolve such outerportion of the preliminary film which actually contains the impurities, and to leave the inner portion of the film adhering to the electrode.
  • a third method of obtaining the same or similar results is the following:
  • the electrode, without preliminary cleaning, is placed in the forming tank which contains an alkaline electrolyte,for instance, borax.
  • Current is now applied, whereby a film is formed on the electrode but partly attacked by the borax..
  • electrolyte is made slightly acidic by addition of boric acid and the electrode subjected to the regular formatiomprocess.
  • a fourth method issimilar to the third and consists in placing the electrode without preliminary cleaning in the forming tank, which again comprises an alkaline solution as caustic soda, but instead of applying a forming current,
  • the caustic soda is left chemically to clean the aluminum-preferably inthe presence of inhibitive agents-as described in connection with the first method.- After a short; period of alkaline cleaning of the electrode, the electrolyte is made acidic, for instance, by addition of boric acid and the forming process undertaken in the regular way.
  • grade A aluminum having 99.6% to 99.7% aluminum is subjected to corrosion in air, an aluminum of 99.9% or higher purity, does not corrode in air.
  • 'Electrodes made ofthis material can be cleaned from adherent contaminationsby means of an organic solvent and no further special precaution is required to prevent the electrode from corrodingin airbefore it is subjected toforma'tion.

Description

STATES PATEN OFFICE 2,067,703 ELECTROLYTIC DEVICE Preston Robinson and Joseph L. Collins, North Adams, Mass, assignors to Sprague Specialties 00., Quincy, Mass, a corporation of Massachusetts No Drawing.
Application March 28, 1931,
Serial No. 526,118
2 Claims. (Cl. 175315) Our invention relates to electrolytic devices, such as electrolytic condensers, rectifiers, or the like, comprising film-forming electrodes.
In such devices use is made of the film-forming effect exhibited by certain metals, for in stance aluminum which, when placed in suitable electrolytes, upon application of the proper voltage are covered with a film. Such films consist of partially hydrated aluminum oxide and have a uni-directional character.
We shall describe our invention in its application to electrolytic condensers, using aluminum electrodes, although it should be well understood that our invention is not limited to such devices or electrode material.
We have found that the oxide layer which forms on aluminum, when exposed to the action of acids or to air, While chemically similar to the substance of the film built up in the electrolytic forming process, substantially differs therefrom in its insulating and dielectric properties. We
v have also found that if an aluminum electrode,
been prevented.
It is, therefore, one object of our invention to provide films of improved qualities by preventing oxidization of the electrode surface prior to the formation of the film.
Other objects of our invention will the specification progresses.
As in the manufacture and handling of the electrodes impurities such as filings, grease, etc., are deposited on and adhere to the electrode surface, the deleterious influences of which are well recognized, it is practice to clean the electrodes before subjecting them to the film-forming process.
In the past, such cleaning was effected by subjecting the aluminum electrodes to an aqueous acidic bath and subsequently rinsing them. in water. However, the acid while removing the impurities from the surface of the aluminum, also dissolves the outer layer of aluminum, and
appear as deleteriously affects the quality of the dielectric film.
We have found that by immersing the aluminum in a properly prepared alkaline solution, we can remove the impurities just as effectively as with an acidic cleanser without forming an oxide layer on the aluminum.
Attempts to use alkaline cleansersfor such p pose, have been unsuccessful so far, because an excessive amount of alkaline was required to properly clean the electrode. In addition, the alkaline attacked and pitted the aluminum to such an extent, particularly around metal impurities in the surface, that it was unfeasible to form a good quality film on the electrodes so cleaned, particularly in the neighborhood of the exposed impurities.
To prevent pitting of the aluminum, it has been suggested to treat the anodes in a weakly alkaline solution, such as borax or trisodium phosphate which will'attack aluminum oxide or hydroxide, but which will not strongly attack aluminum. However, in order to obtain complete cleaning with such reagents, it would be necesdium phosphate, sodium meta-silicate, sodium fluoride, etc. The strong local actionof the alkali is hereby transformed into an evenly distributed moderate action and the aluminum, instead of being pitted and damaged in spots, is evenly etched over its whole surface. At the same time, only a small amount of caustic reagent is required.
Thusbyusing a caustic cleanser in the presence ofiproper inhibiting agents, objectionable oxidization of the electrode is prevented, and at the same time through evenly distributed etching of the aluminum surface, the eifective area of the electrode is considerably increased.
' After their cleaning in a caustic solvent, the electrodes are preferably subjected to rinsing.
However, we have found that objectionable oxidization of the electrode before it is formed is not fully prevented even by alkaline cleaning because, as above stated, the cleaned electrode when left exposed to air, oxidizes on its surface and this due to thewater presentformsan oxide layer oxide layer is just as objectionable as the oxide through rinsing and its presence, as stated above,
on the electrode. This oxide layer is not removed film formed in an acidic cleaner.
Even relatively short exposures to air of the other to the forming process immediately afterits cleaning, we have found the following:
The capacity of the condenser using the first electrode was 6.2 MFD and its power factor 24%, while of the condenser using the second electrode, the capacity was 7.1 MFD and the power factor 15%.
In practice, therefore, after We have cleaned the electrodes in a proper alkaline solution and subsequently rinsed them preferably in a very weak alkaline solution-as a diluted solution of borax-we transfer the electrodes from the bathimmediately into the forming tank and subject them therein immediately to formation, whereby the electrolyte used in the formation process is preferably slightly acidic.
Instead of using the above described method, we have-found that undesirable oxidization of the electrode can be prevented bya second method as follows! The electrodes, instead of being subjected to a preliminary chemical cleaning, undergo a preliminary forming process, which consists of placing the electrodes in a slightly acidic electrolyte, for instance, borax and boric acid in which the electrodes are subjected to a short formation. As a result of this formation, a thin oxide film covers the electrode, which film also includes the surface contaminations of the aluminum.
After such preliminary formation, the electrodes are submerged in an alkaline solution, for instance, borax, sodium phosphate, etc., which attacks and removes the preliminary film without oxidizing or attacking the aluminum. Thereafter, the electrodes are subjected to the regular forming process, preferably in a slightly acidic electrolyte.
In using this method, it is-sometimes found advisable to have .the alkaline solution only dissolve such outerportion of the preliminary film which actually contains the impurities, and to leave the inner portion of the film adhering to the electrode.
. A third method of obtaining the same or similar results is the following: The electrode, without preliminary cleaning, is placed in the forming tank which contains an alkaline electrolyte,for instance, borax. Current is now applied, whereby a film is formed on the electrode but partly attacked by the borax..
Thereafter the electrolyte is made slightly acidic by addition of boric acid and the electrode subjected to the regular formatiomprocess.
A fourth method issimilar to the third and consists in placing the electrode without preliminary cleaning in the forming tank, which again comprises an alkaline solution as caustic soda, but instead of applying a forming current,
the caustic soda is left chemically to clean the aluminum-preferably inthe presence of inhibitive agents-as described in connection with the first method.- After a short; period of alkaline cleaning of the electrode, the electrolyte is made acidic, for instance, by addition of boric acid and the forming process undertaken in the regular way.
We have also found that while the highest 1 quality commercially available aluminum, the
so-called grade A aluminum, having 99.6% to 99.7% aluminum is subjected to corrosion in air, an aluminum of 99.9% or higher purity, does not corrode in air. 'Electrodes made ofthis material can be cleaned from adherent contaminationsby means of an organic solvent and no further special precaution is required to prevent the electrode from corrodingin airbefore it is subjected toforma'tion.
In the foregoing we have described various methods to prevent objectionable oxidation of aluminum electrodes during or subsequent to their cleaning and to obtain higher quality oxide films. While we have illustrated our invention in connection with electrolytic condensers, using aluminum electrodes, and, described specific methods, we do not wish to be limited to such devices, material or methods, but desire the appended claims to beconstrued as broad as permissible in view of the prior art.
Since claims relating to the second and third method hereinabove described are made in our Patent #2,035,022, of March '24, 1936,'which issued on' anapplication, Ser. No. 1,432, filed January 11, 1935, as a division of the present application, claims to said second and third methods are not madeherein. 9
What we, therefore, claimand desire to secure by Letters Patent is:
, 1. In the manufacture of aluminum electrodes and subjecting the electrode to film formationin the solution of borax and boric acid.
. PRESTON ROBINSON.
JOSEPH L. COLLINS.
US526118A 1931-03-28 1931-03-28 Electrolytic device Expired - Lifetime US2067703A (en)

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Application Number Priority Date Filing Date Title
US526118A US2067703A (en) 1931-03-28 1931-03-28 Electrolytic device
US1432A US2035022A (en) 1931-03-28 1935-01-11 Electrolytic device

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US2067703A true US2067703A (en) 1937-01-12

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4126483A (en) * 1977-06-03 1978-11-21 Ford Motor Company Method of adherency of electrodeposits on light weight metals
US4225397A (en) * 1978-11-06 1980-09-30 Ford Motor Company New and unique aluminum plating method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4126483A (en) * 1977-06-03 1978-11-21 Ford Motor Company Method of adherency of electrodeposits on light weight metals
US4225397A (en) * 1978-11-06 1980-09-30 Ford Motor Company New and unique aluminum plating method

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