GB2036432A - Improvements in or Relating to Electrolyte Capacitors - Google Patents
Improvements in or Relating to Electrolyte Capacitors Download PDFInfo
- Publication number
- GB2036432A GB2036432A GB7939873A GB7939873A GB2036432A GB 2036432 A GB2036432 A GB 2036432A GB 7939873 A GB7939873 A GB 7939873A GB 7939873 A GB7939873 A GB 7939873A GB 2036432 A GB2036432 A GB 2036432A
- Authority
- GB
- United Kingdom
- Prior art keywords
- anode
- seal
- capacitor
- tantalum
- lead
- 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.)
- Granted
Links
- 239000003990 capacitor Substances 0.000 title claims abstract description 37
- 239000003792 electrolyte Substances 0.000 title claims abstract description 16
- 238000000034 method Methods 0.000 claims abstract description 12
- 238000003825 pressing Methods 0.000 claims abstract description 8
- 230000032683 aging Effects 0.000 claims abstract description 4
- 238000007789 sealing Methods 0.000 claims description 9
- 239000011521 glass Substances 0.000 abstract description 9
- 230000002035 prolonged effect Effects 0.000 abstract 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 34
- 229910052715 tantalum Inorganic materials 0.000 description 27
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 238000010276 construction Methods 0.000 description 7
- 238000003466 welding Methods 0.000 description 5
- 239000000843 powder Substances 0.000 description 4
- 238000005245 sintering Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000002048 anodisation reaction Methods 0.000 description 2
- 238000007743 anodising Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- HEPLMSKRHVKCAQ-UHFFFAOYSA-N lead nickel Chemical compound [Ni].[Pb] HEPLMSKRHVKCAQ-UHFFFAOYSA-N 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 229910000679 solder Inorganic materials 0.000 description 2
- 229910052779 Neodymium Inorganic materials 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000010407 anodic oxide Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000000712 assembly Effects 0.000 description 1
- 238000000429 assembly Methods 0.000 description 1
- 230000003190 augmentative effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007499 fusion processing Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000007373 indentation Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- QEFYFXOXNSNQGX-UHFFFAOYSA-N neodymium atom Chemical compound [Nd] QEFYFXOXNSNQGX-UHFFFAOYSA-N 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 239000010955 niobium Substances 0.000 description 1
- GUCVJGMIXFAOAE-UHFFFAOYSA-N niobium atom Chemical compound [Nb] GUCVJGMIXFAOAE-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- -1 polytetrafluorethylene Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000009966 trimming Methods 0.000 description 1
- 238000004018 waxing Methods 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01G—CAPACITORS; CAPACITORS, RECTIFIERS, DETECTORS, SWITCHING DEVICES, LIGHT-SENSITIVE OR TEMPERATURE-SENSITIVE DEVICES OF THE ELECTROLYTIC TYPE
- H01G9/00—Electrolytic capacitors, rectifiers, detectors, switching devices, light-sensitive or temperature-sensitive devices; Processes of their manufacture
- H01G9/004—Details
- H01G9/08—Housing; Encapsulation
- H01G9/10—Sealing, e.g. of lead-in wires
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Fixed Capacitors And Capacitor Manufacturing Machines (AREA)
Abstract
An electrolytic capacitor is assembled by introducing the cathode anode and electrolyte into a can 1 and by pressing the anode lead 5 into the anode 10. The anode lead is provided with a primary seal including a glass pre-form 6. A secondary seal in the form of a bung 8 and O-ring 7 is also provided to separate the electrolyte from the glass 6 provide an anti- vibration mount while the glass is being melted e.g. by a laser beam. Before the anode lead is pressed into the anode body it is machined to produce a barbed portion 15 which, during pressing, strips off anodically formed oxide to give a good electrical contact. The damage to the anode caused by the pressing operation is subsequently repaired by a prolonged ageing process. <IMAGE>
Description
SPECIFICATION
Improvements in or Relating to Electrolyte
Capacitors
The present invention relates to electrolytic capacitors having, for example, tantalum anodes and more particularly relates to the hermetic sealing of such capacitors.
Electrolytic capacitor assemblies with the nonsolid electrolytes comprise a container into which a capacitor anode is placed. The interior wall of the container also serves as the cathode, the capacitance of which can be augmented by any treatment which will increase the surface area.
Hitherto, hermetic glass-to-metal seals have been constructed as follows: a central tubular metal eyelet is circumscribed by a glass ring which is sealed thereto, and a metal washer circumscribes the glass ring and is sealed thereto.
The anode lead wire is positioned so that it passes up the metal eyelet. The glass-to-metal seal is positioned in the end of the capacitor can and soldered at its periphery to the can wall, which is usually of silver.
Two possible methods are employed for sealing the anode wire:
(a) anode has tantalum wire already sintered in. The tantalum wire is welded to a solderable nickel lead. The weld area is enclosed within the solderable tube of the glass-metal seal, and the seal is completed by filling this tube with solder.
(b) anode has tantalum wire already sintered in. The tantalum wire is cropped off at the top of the tantalum tube which forms the centre of the glass-metal seal. The tube and wire are welded together to complete the hermetic seal. A solderable nickel lead is welded to the outside of the tantalum tube.
The present invention provides an electrolyte capacitor including an anode mounted substantially concentrically within an annular shaped cathode and separated therefrom by an electrolyte, contained within a can surrounding the cathode, the can being a holiow construction initially open at one end for insertion of the cathode and anode structures, the anode being provided with an aperture for reception of anode lead; a seal for sealing the open end of the can, the seal including means for connecting the anode lead through the seal in electrical isolation from the can, and including a further sealing means within said can comprising a bung which is tightly fitted to surround the anode lead, said further seal, being positioned between the anode and seal and preventing the electrolyte from contacting the seal at least during the sealing operation.
In a first preferred embodiment the can and anode are of tantalum and in a second preferred embodiment they are wholly or partly of niobium.
The anode is preferably coated with a dielectric oxide film. The electrolyte is preferably of either aqueous sulphuric acid or lithium chloride solution, or either of these two containing a gelling agent.
The cathode is preferably a highly porous sleeve of sintered tantalum powder crimped, welded or sintered into the tantalum casing of the capacitor.
The anode lead is preferably of tantalum and the seal is a tantalum lead-glass-tantalum ring seal which is affixed to the tantalum case by high energy beam, plasma arc, resistance weld or other suitable means.
The bung is preferably of polytetrafluorethylene and the "0" ring preferably of a fluorinated elastomer. The bung and "0" ring assembly not only isolate the electrolyte during the welding operation but provide a top anode support and an anti-vibration mount.
The present invention also provides a method of assembling an electrolytic capacitor in which an annular sleeve shaped cathode is inserted into the open end of a can, in which an anode structure is inserted into said can in a spaced apart relationship from said cathode, the space between said anode and cathode being filled with an electrolyte, said anode structure having an aperture for reception of an anode lead; in which a primary seal, for sealing the open end of the can, and comprising an anode lead electrically isolated from the rest of the seal is formed, in which a secondary seal is positioned on the anode lead on the inside face of said primary seal to form a seal between said anode lead and said can prior to sealing of the primary seal of said capacitor, in which the end of the anode lead projecting from said secondary seal is machined to provide projections on said lead, in which said capacitor is assembled by forcing the projecting portion of said anode lead into said anode until the primary seal is in position, in which said primary seal is welded round its periphery to said can and in which said capacitor is subjected to an ageing process to restore any damage to said anode and anode lead structure incurred during said pressing operation.
Embodiments of the present invention will now be described by way of example with reference to the accompanying drawings in which: Figure 1 shows a sectional view of the completed capacitor showing the novel seal construction,
Figure 2 shows a portion of the capacitor of
Figure 1,
Figure 3 shows a first closure member for the capacitor of Figure 1,
Figure 4 shows a second closure member for the capacitor of Figure 1,
Figure 5 shows a partial construction of the seal structure of the capacitor of Figure 1 illustrating the method of construction and,
Figure 6 shows a further stage in the construction of the capacitor of Figure 1.
Referring now to Figures 1 and 2 of the drawing, the capacitor inciudes a concentric sleeve 2 of tantalum powder which, when mechanically secured sintered or welded into the tantalum container 1 provides a cathode of greatly enhanced surface area (Figure 2). The outer tantalum container 1 is produced by blanking out a disc from tantalum strip and deep drawing this into the form of a can. The sleeve 2 is made either by freezing a tantalum powderliquid mixture in a rubber mould, followed by drying and sintering, or by pressing a tantalum powder or powder-wax mixture in a steel mould, followed by dewaxing (if necessary) and sintering.
The porous sleeve 2 may be secured to the outer can by mechanical constriction of the can, by welding, or by vacuum-sintering the sleeve and the can together. A solderable wire 3 is welded axially to the base of the can to provide the negative lead. The interior of the can 1 with its concentric sleeve 2 is anodised to provide a D.C.
reverse voltage capability.
The tantalum-glass-tantalum seal of which possible forms are shown in Figures 3 and 4 is produced from three constituent parts. Item 4 is a centrally-pierced tantalum cup, prepared by blanking and shaping tantalum strip. Item 5 is a tantalum stud prepared from tantalum wire, while item 6 is a glass preform prepared from an acidresisting glass. The glass-tantalum seal can be matched seal, using a glass having a coefficient of expansion similar to that of tantalum, or a compression seal. A fusion process is preferably employed in which chemical bonding takes place.
The parts are assembled in a jig and heated in an evacuated furnace to between 1 2500C and 14000C; argon is introduced and heating continued. After the initial fusion, a reaction takes place between the metal oxide and the constituents of the glass, producing a seal having very satisfactory mechanical and electrical properties. This method of preparing the glass-tometal seal is the subject of British Patent No.
1,421,050.
In a practical capacitor the annular sleeve of Ta powder forming the cathode is manufactured as follows:
A high-capacitance tantalum powder, typically 4 micron particle size, is mixed with wax and pressed to a density of 6.5 to 8.5 g/cc; pressing can be accomplished separately in a die or by using the can as a die.
After the separate pressing operation, the cathode sleeve is pushed into the tantalum can.
Can and sleeve are heated to between 1 900 and 4500C under vacuum to remove the wax binder. On de-waxing, the sleeve expands slightly and so is held in the can.
The wall of the can may be etched, prior to insertion of the cathode powder to improve adhesion. Care must be taken not to etch the seal area at the mouth of the can.
Agglomerated powders or binderless powders may also be used for producing the cathode sleeve. A final fired density of 4.5 to 7.0 g/cc is achievable.
The cathode sleeve and can combination is anodised to between 4.5 and 7 V D.C., to withstand a reverse voltage of 3.0 V. Anodisation is carried out in a tantalum jig and the cans are kept vertical to allow the gases produced to escape.
For applications not requiring a reverse voltage capability greater than 1 V D.C. a platinum or ruthenium paint may be applied and fired on to the interior. Such methods are the subject of a
Plessey (U.K.) Limited, Patent No. 1,317,494.
In a practical embodiment the tantalum can is produced using 0.010 in thick tantalum strip, normal or grain-stabilised. The tantalum strip is degreased just prior to anodising for a period of 1 5 minutes at 250C within a voltage range of 30 to 100 V D.C. The materiai is blanked and the can is produced from the blank using a minimum of five drawing stages including trimming to length.
Any high-pressure grade of deep-drawing lubricant can be employed, this is removed by degreasing and the can is fired in a radiofrequency furnace to remove all traces of the oxide film.
In a practical embodiment the central tantalum wire of the glass-to-metal seal is cleaned, prior to anodising, by immersion in a chemical etching solution. The wires are anodised to 200 V at 850C (or the equivalent voltage if another temperature is employed).
The cylindrical porous anodes are pressed by conventional means and sintered in the temperature range of 1600 to 20500 C. The density range is typicaliy 6.5 g/cc to 10.5 g/cc.
Anodisation is carried out in a tantalum expanded metal basket; the applied voltage is raised progressively to at least 140% of the intended working voltage.
The electrolyte capacitor is assembled as described in the following steps:
(a) The portion of the central wire below the cup of the glass-to-tantalum hermetic seal is anodised to 200 V to provide a high-quality dielectric film.
(b) The anodised portion of the wire (5) is dipped into a viscous wire sealant.
(c) The "0" ring and bung assembly (7, 8) is pushed on the anodised portion of the wire until it rests up against the tantalum cup - see Figure 5.
(d) The protruding portion of the anodised wire is operated upon by a press tool which produces knurled or barb-like indentations 1 5 in the surface - see Figure 6.
(e) The cathode sleeve (2) and anode (10) are saturated with electrolyte, and electrolyte is dispensed into the cathode can.
(f) The bottom anode support (11) is positioned on the base of the anode, which is inserted centrally into the cathode sleeve and can assembly. A locating tool is used to ensure that the anode is inserted concentrically.
(g) The glass-to-metal assembly, fitted with "0" ring and bung, is positioned on top of the can (the "0" ring resting on the belled-out portion).
The capacitor parts are put on a tool in a toggle press and a vacuum applied to an enclosure surrounding the tool. The "0" ring is pushed down level and the vacuum is released.
During this operation the barbed portion of the central wire is forced into the central hole of the anode, stripping off sufficient of the anodically formed oxide to give good electrical contact. The central hole in the anode is slightly tapered and the wire is, therefore, secured mechanically within the anode block.
(h) The top of the can is turned in by about 5O to the vertical. This provides a tight, compact joint suitable for welding, as well as keeping the anode and wire under compression.
(i) The top of the can is welded to the adjacent top of the cup of the glass-to-metal seal assembly, by mounting the capacitor in a clamp and rotating it under the beam of high-energy radiation until the weld is completed.
(j) The capacitor is completed by welding a solderable lead (12) to the anode wire where it protrudes outwardly above the welded glass-tometal seal.
(k) Healing of the anodic oxide film, damaged when the barbs on the central wire were driven into the central hole of the anode, is accomplished by an ageing process (or burning) during which the capacitor is subjected to a full rated voltage - at the upper operating temperature, for a period between 8 and 60 hours.
Welding Details
The capacitor is put in a clamp and rotated below a laser beam.
With a carbon dioxide laser, a wavelength band around 10.6 micro metre is employed, in continuous mode. A speed of 4 to 5 secs per revolution is used.
An output of 380 to 400 watts is typical (e.g.
Ferranti 400 watt laser, MF400) Alternatively a
Neodymium solid state laser can be used. This has a wavelength band of 1.06 micrometer, and supplies 4 to 60 Joules of energy per pulse.
Between 2 and 4 pulses per second are used, with a pulse length of 2.75 millisecond.
The rotational speed of the capacitor clamp can be between 30 sec and 90 sec per revolution.
The advantages of the present capacitor are that no solder is used in its construction and, therefore, no corrosion is possible. Since there is no weld at the top of the narrow tantalum tube used in previous constructions there is no chance of thermal oxide being produced. This is an advantage since it has been found that thermal oxide in contact with electrolyte leads to degradation of the electrical characteristics of the capacitor.
Claims (3)
1. A method of assembling an electrolytic capacitor in which an annular sleeve shaped cathode is inserted into the open end of a can, in which an anode structure is inserted into said can in a spaced apart relationship from said cathode, the space between said anode and cathode being filled with an electrolyte, said anode structure having an aperture for reception of an anode lead in which a primary seal, for sealing the open end of the can, and comprising an anode lead electrically isolated from the rest of the seal is formed in which a secondary seal is positioned on the anode lead on the inside face of said primary seal to form a seal between said anode lead and said can prior to sealing of the primary seal of said capacitor, in which the end of the anode lead projecting from said secondary seal is machined to provide projections on said lead, in which said capacitor is assembled by forcing the projecting portion of said anode lead into said anode until the primary seal is in position, in which said primary seal is welded round its periphery to said can and in which said capacitor is subjected to an ageing process to restore any damage to said anode and anode lead structure incurred during said pressing operation.
2. An electrolytic capacitor constructed in accordance with the method of Claim 1.
3. A method of assembling an electrolytic capacitor substantially as described with reference to the accompanying drawings.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US05/961,919 US4296458A (en) | 1977-11-24 | 1978-11-20 | Electrolyte capacitors with improved anode-to-lead connection |
Publications (2)
Publication Number | Publication Date |
---|---|
GB2036432A true GB2036432A (en) | 1980-06-25 |
GB2036432B GB2036432B (en) | 1983-07-06 |
Family
ID=25505184
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7939873A Expired GB2036432B (en) | 1978-11-20 | 1979-11-19 | Electrolyte capacitors |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB2036432B (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9737724B2 (en) | 2011-02-04 | 2017-08-22 | Vishay Sprague, Inc. | Hermetically sealed electrolytic capacitor |
US11189431B2 (en) | 2018-07-16 | 2021-11-30 | Vishay Sprague, Inc. | Low profile wet electrolytic tantalum capacitor |
US11742149B2 (en) | 2021-11-17 | 2023-08-29 | Vishay Israel Ltd. | Hermetically sealed high energy electrolytic capacitor and capacitor assemblies with improved shock and vibration performance |
-
1979
- 1979-11-19 GB GB7939873A patent/GB2036432B/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9737724B2 (en) | 2011-02-04 | 2017-08-22 | Vishay Sprague, Inc. | Hermetically sealed electrolytic capacitor |
US11189431B2 (en) | 2018-07-16 | 2021-11-30 | Vishay Sprague, Inc. | Low profile wet electrolytic tantalum capacitor |
US11742149B2 (en) | 2021-11-17 | 2023-08-29 | Vishay Israel Ltd. | Hermetically sealed high energy electrolytic capacitor and capacitor assemblies with improved shock and vibration performance |
Also Published As
Publication number | Publication date |
---|---|
GB2036432B (en) | 1983-07-06 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
732 | Registration of transactions, instruments or events in the register (sect. 32/1977) | ||
PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 19921119 |