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(11) |
EP 0 000 965 B1 |
| (12) |
EUROPEAN PATENT SPECIFICATION |
| (45) |
Mention of the grant of the patent: |
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03.09.1980 Bulletin 1980/18 |
| (22) |
Date of filing: 31.07.1978 |
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Cathode foil for electrolytic capacitors
Kathodenfolie für Elektrolytkondensatoren
Feuille cathodique pour condensateurs électrolytiques
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Designated Contracting States: |
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BE CH DE FR GB NL |
| (30) |
Priority: |
22.08.1977 NL 7709231
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| (43) |
Date of publication of application: |
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07.03.1979 Bulletin 1979/05 |
| (71) |
Applicant: Philips Electronics N.V. |
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5621 BA Eindhoven (NL) |
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| (72) |
Inventors: |
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- Van Herwijnen, Arend
NL-5600 Eindhoven (NL)
- Vogel, Pieter Marten
NL-5600 Eindho ven (NL)
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| (74) |
Representative: Jelmorini, Pius Antonius et al |
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INTERNATIONAAL OCTROOIBUREAU B.V.
Prof. Holstlaan 6 5656 AA Eindhoven 5656 AA Eindhoven (NL) |
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| Note: Within nine months from the publication of the mention of the grant of the European
patent, any person may give notice to the European Patent Office of opposition to
the European patent
granted. Notice of opposition shall be filed in a written reasoned statement. It shall
not be deemed to
have been filed until the opposition fee has been paid. (Art. 99(1) European Patent
Convention).
|
[0001] The invention relates to aluminium foil for electrolytic capacitors and to cathode
foil in particular and to electrolytic capacitor manufactured with this foil.
[0002] An electrolytic aluminium foil capacitor consists of an anode foil of aluminium provided
with a dielectric aluminium oxide skin obtained by anodic oxidation and an etched
cathode foil of aluminium which are rolled together with a so-called separator of
an insulating material to form a wound body. The wound body is impregnated with an
electrolyte liquid and encapsulated.
[0003] It is important that the desired capacitance is concentrated on as small a surface
area as possible, which means that the metal surface area to be oxidized (forming)
must be as large as possible. To this end the surface of the aluminium foil obtained
by rolling is subjected to an etching operation. Etching is usually performed electrolytically.
To obtain a high capacitance per unit of surface area it is important that the surface
area of the cathode foil, which is encapsulated in normal capacitors in a non-formed
state, is also enlarged and that in the order of magnitude of the anode foil.
[0004] Aluminium of a very high purity, namely AI 99.99% is usually used for the anode foil.
[0005] According to US Specification 3,899,723 cathode foil consisting of an aluminium-manganese
alloy having a manganese content of 0.2 to 2 weight % is used in an advantageous manner.
Besides the fact that this foil has a high capacitance value after etching, so that
after assembly with a formed anode foil it furnishes a capacitor having a high CV
value, it has, prior to etching, a high impact strength and so the foil suffers less
damage when handled prior to, during and after the etching operation compared to foil
to which no manganese is added. The specification of this type of alloy having 0.9-1.4%
Mn in accordance with the DIN standard 1725, page 1, stipulates the following maximum
values for contaminations:

[0006] However, the effects aimed at did not appear to be quite optimal and it was therefore
an object of the invention to obtain a further increase in the capacitance value and
a still higher impact strength of the foil after etching.
[0007] The cathode foil according to the invention is therefore characterized in that it
has next to a manganese content of between 0.2 and 2 weight % a copper content of
between 0.15 and 5.3 weight %.
[0008] In accordance with a further elaboration of the invention an increase in the impact
strength in particular is obtained if furthermore the titanium content of the cathode
foil is between 0.03 and 0.5 weight %.
[0009] Preferably the Mn is between 0.5 and 1.5%, Cu between 0.15 and 0.5 and Ti between
0.05 and 0.25 weight %.
[0010] Compared to the foil in accordance with the above-mentioned US Patent Specification
3,899,723 the foil according to the invention has a 20 to 30% higher capacitance after
etching with a given number of Coulombs/cm
2 and, furthermore, an impact strength after etching with a given number of Coulombs/cm
2 which is approximately a factor of 2 higher.
[0011] The latter fact enables an increased through-etching of the foil so that an additional
increase of the capacitance is possible, or the choice of a thinner foil as a starting
material.
Example 1
[0012] By way of non-limitative example there now follows a comparison between foil in accordance
with the above-mentioned DIN specification (1) and foil according to the invention
(2). The relevant compositions in % by weight are:

[0013] Both foils, having a thickness of 60 µm were electrolytically etched in an aqueous
solution of 250 g/I NaCI at different numbers of Coulombs/cm
2.
[0014] The capacitance values were measured in a liquid consisting of a 5% solution of ammonium-
pentaborate in water (resistivity 100 Q.cm) versus a silver-plated counter electrode.
The impact strength after etching was determined.
[0015] In Figure 1 of the accompanying drawing the capacitance measured (C in µF/cm
2) and the impact strength σ measured (in mJ/15 mm foil width) of the two foils (1)
and (2) are plotted versus the number of etching Coulombs Q per cm
2.
[0016] The pronounced improvement achieved by the measure according to the invention, particularly
in the practically suitable range of etching charges between 10 and 50 Coulombs/cm
2 is very spectacular. When using the cathode foil according to the invention together
with anode foil, a spacer and an electrolyte solution in a complete electrolytical
capacitor the capacitance value per volume will be found to be correspondingly higher.
Example 2
[0017] Foils were produced which, starting from Al - 99.99%, contained 1% Mn and increasing
quantities of Cu from 0 to 0.4%. Etching and capacitance measurement were performed
as described in example 1. Figure 2 shows the values of the capacitance (C in µF/cm
2) versus the Cu-content (in weight %).
1. A cathode foil of aluminium for electrolytical capacitors consisting of an aluminium-manganese
alloy having a Mn-content between 0.2 and 2 weight %, characterized in that furthermore
the alloy has a copper content of between 0.15 and 5.3 weight %.
2. A cathode foil as claimed in Claim 1, characterized in that the titanium content
thereof is between 0.03 and 0.5 weight %.
3. A cathode foil as claimed in Claim 2, characterized in that the copper content
thereof is between 0.15 and 0.5 and the titanium content between 0.05 and 0.25 weight
%.
4. An electrolytical foil capacitor in which the cathode consists of etched foil as
claimed in Claim 1, 2 or 3.
1. Kathodenfolie aus Aluminium für Elektrolytkondensatoren, die aus einer Aluminium
- Mangan - Legierung mit einem Mangangehalt zwischen 0,2 und 2 Gew.% besteht, dadurch
gekennzeichnet, dass die Legierung ausserdem einen Kupfergehalt zwischen 0,15 und
5,3 Gew.% aufweist.
2. Kathodenfolie nach Anspruch 1, dadurch gekennzeichnet, dass der Titangehalt derselben
zwischen 0,03 und 0,5 Gew.% liegt.
3. Kathodenfolie nach Anspruch 2, dadurch gekennzeichnet, dass ihr Kupfergehalt zwischen
0,15 und 0,5 und ihr Titangehalt zwischen 0,05 und 0,25 Gew.% liegt.
4. Elektrolytischer Folienkondensator, in dem die Kathode aus gebeizter Folie nach
Anspruch 1, 2 oder 3 besteht.
1. Feuille cathodique en aluminium pour condensateurs électrolytiques, constituée
par un alliage en aluminium-manganèse, présentant une teneur en manganèse comprise
entre 0,2 et 2% en poids, caractérisée en ce que l'alliage contient en outre une teneur
en cuivre comprise entre 0,15 et 5,3% en poids.
2. Feuille cathodique selon la revendication 1, caractérisée en ce que la teneur en
titane est comprise entre 0,03 et 0,5% en poids.
3. Feuille cathodique selon la revendication 2 caractérisée en ce que la teneur en
cuivre est comprise entre 0,15 et 0,5 et la teneur en titane entre 0,05 et 0,25% en
poids.
4. Condensateur à feuille électrolytique dont la cathode est constituée par une feuille
décapée suivant la revendication 1, 2 ou 3.