WO2009113123A1 - 電解コンデンサ用アルミニウム電極板の製造方法 - Google Patents
電解コンデンサ用アルミニウム電極板の製造方法 Download PDFInfo
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- WO2009113123A1 WO2009113123A1 PCT/JP2008/000529 JP2008000529W WO2009113123A1 WO 2009113123 A1 WO2009113123 A1 WO 2009113123A1 JP 2008000529 W JP2008000529 W JP 2008000529W WO 2009113123 A1 WO2009113123 A1 WO 2009113123A1
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- etching
- aluminum
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- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 96
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 92
- 239000003990 capacitor Substances 0.000 title claims abstract description 46
- 238000000034 method Methods 0.000 title claims description 31
- 230000008569 process Effects 0.000 title claims description 17
- 238000005530 etching Methods 0.000 claims abstract description 162
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 37
- 239000000654 additive Substances 0.000 claims abstract description 31
- 230000000996 additive effect Effects 0.000 claims abstract description 29
- 239000010949 copper Substances 0.000 claims abstract description 24
- 229910052742 iron Inorganic materials 0.000 claims abstract description 17
- 229910052802 copper Inorganic materials 0.000 claims abstract description 16
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 claims abstract description 14
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000004519 manufacturing process Methods 0.000 claims abstract description 12
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims abstract description 7
- BJQHLKABXJIVAM-BGYRXZFFSA-N 1-o-[(2r)-2-ethylhexyl] 2-o-[(2s)-2-ethylhexyl] benzene-1,2-dicarboxylate Chemical compound CCCC[C@H](CC)COC(=O)C1=CC=CC=C1C(=O)OC[C@H](CC)CCCC BJQHLKABXJIVAM-BGYRXZFFSA-N 0.000 claims abstract description 3
- BJQHLKABXJIVAM-UHFFFAOYSA-N Diethylhexyl phthalate Natural products CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229960003330 pentetic acid Drugs 0.000 claims abstract description 3
- 239000002738 chelating agent Substances 0.000 claims description 18
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 claims description 10
- 239000012535 impurity Substances 0.000 claims description 9
- 230000009471 action Effects 0.000 claims description 7
- URDCARMUOSMFFI-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(2-hydroxyethyl)amino]acetic acid Chemical compound OCCN(CC(O)=O)CCN(CC(O)=O)CC(O)=O URDCARMUOSMFFI-UHFFFAOYSA-N 0.000 claims description 6
- DLYUQMMRRRQYAE-UHFFFAOYSA-N tetraphosphorus decaoxide Chemical compound O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 claims description 6
- 239000004471 Glycine Substances 0.000 claims description 5
- 235000019832 sodium triphosphate Nutrition 0.000 claims description 3
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 claims description 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000000243 solution Substances 0.000 description 40
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 24
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 20
- 238000011282 treatment Methods 0.000 description 17
- 239000007864 aqueous solution Substances 0.000 description 9
- 229910000765 intermetallic Inorganic materials 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 238000004090 dissolution Methods 0.000 description 8
- 230000005611 electricity Effects 0.000 description 8
- 229920000128 polypyrrole Polymers 0.000 description 7
- 229910052710 silicon Inorganic materials 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 229920001002 functional polymer Polymers 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- FSVCELGFZIQNCK-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)glycine Chemical compound OCCN(CCO)CC(O)=O FSVCELGFZIQNCK-UHFFFAOYSA-N 0.000 description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 4
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 238000005096 rolling process Methods 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000007784 solid electrolyte Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229920000123 polythiophene Polymers 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 229940080299 sodium 2-naphthalenesulfonate Drugs 0.000 description 2
- YWPOLRBWRRKLMW-UHFFFAOYSA-M sodium;naphthalene-2-sulfonate Chemical compound [Na+].C1=CC=CC2=CC(S(=O)(=O)[O-])=CC=C21 YWPOLRBWRRKLMW-UHFFFAOYSA-M 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- FLDCSPABIQBYKP-UHFFFAOYSA-N 5-chloro-1,2-dimethylbenzimidazole Chemical compound ClC1=CC=C2N(C)C(C)=NC2=C1 FLDCSPABIQBYKP-UHFFFAOYSA-N 0.000 description 1
- 229910018084 Al-Fe Inorganic materials 0.000 description 1
- 229910018192 Al—Fe Inorganic materials 0.000 description 1
- 229910018191 Al—Fe—Si Inorganic materials 0.000 description 1
- 239000001741 Ammonium adipate Substances 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- -1 aluminum ions Chemical class 0.000 description 1
- 235000019293 ammonium adipate Nutrition 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 238000007743 anodising Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000013522 chelant Substances 0.000 description 1
- 238000005097 cold rolling Methods 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000000866 electrolytic etching Methods 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000010191 image analysis Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Images
Classifications
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- 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
- H01G9/04—Electrodes or formation of dielectric layers thereon
- H01G9/048—Electrodes or formation of dielectric layers thereon characterised by their structure
- H01G9/055—Etched foil electrodes
-
- 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
- H01G9/0029—Processes of manufacture
- H01G9/0032—Processes of manufacture formation of the dielectric layer
-
- 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
- H01G9/04—Electrodes or formation of dielectric layers thereon
- H01G9/042—Electrodes or formation of dielectric layers thereon characterised by the material
- H01G9/045—Electrodes or formation of dielectric layers thereon characterised by the material based on aluminium
Definitions
- the present invention relates to a method for producing an aluminum electrode plate for electrolytic capacitors obtained by etching an aluminum plate.
- electrolytic capacitors are required to have lower ESL and higher capacity in addition to lower height, lower impedance, and lower ESR. ing. Solid aluminum electrolytic capacitors have been developed to meet these requirements, but in order to increase the capacity of electrolytic capacitors, it is necessary to increase the etching rate of the aluminum foil.
- the conventional etching technique has a problem that the etching portion is dissolved along with the growth of etching pits, and the etching magnification cannot be increased.
- an object of the present invention is to provide a method for producing an aluminum electrode plate for electrolytic capacitors, which can obtain a high capacitance by improving an etching solution.
- an aluminum plate having an aluminum purity of 99.98% by mass or more, containing less than 30 ppm of copper, and containing 5 to 50 ppm of iron has a chelating action.
- AC etching is performed in an etching solution containing an additive at a concentration of 0.01 ppm or more and less than 100 ppm, the etching magnification can be improved as a result of suppressing dissolution at the surface when growing the etching pits. I got new knowledge that I can do it.
- the present invention has been made on the basis of such knowledge, and in the method for producing an aluminum electrode plate for an electrolytic capacitor in which an aluminum plate is subjected to AC etching in an etching solution to enlarge the surface, the aluminum plate has an aluminum purity. 99.98% by mass or more, containing less than 30 ppm of copper, 5 to 50 ppm of iron, and the balance is composed of other inevitable impurities, and the etching solution contains an additive having a chelating action of 0.01 ppm or more and less than 100 ppm It is characterized by being blended in a concentration.
- aluminum etched plate refers to a thickness of 150 ⁇ m or more.
- an aluminum plate is AC-etched in an etching solution containing an additive having a chelating action at a concentration of 0.01 ppm or more and less than 100 ppm, several thousand to several hundred thousand sponges per square millimeter are used. Shaped pits can be drilled.
- an etching plate there is little dissolution on the surface, and the etching proceeds to a depth of 150 ⁇ m or more in total on both surfaces. More specifically, the etching proceeds to a depth of 75 ⁇ m or more, or 100 ⁇ m or more, and further 120 ⁇ m or more on one side. For this reason, the aluminum electrode plate for electrolytic capacitors with a high etching magnification and a high electrostatic capacity can be obtained.
- etching step for the aluminum plate at least an etching step for generating etching pits in the aluminum plate and an etching step for growing the etching pits, and an etching step for growing the etching pits, It is preferable to perform etching in the etching solution containing an additive.
- the temperature of the etching solution is preferably set to 25 ° C. or lower.
- examples of the additive include DTPA (diethylenetriaminepentaacetic acid), EDTA (ethylenediaminetetraacetic acid), DHEG (diethylhexylphthalate), HEDTA (hydroxyethylethylenediaminetriacetic acid), glycine, phosphorus pentoxide and tripolyphosphoric acid.
- DTPA diethylenetriaminepentaacetic acid
- EDTA ethylenediaminetetraacetic acid
- DHEG diethylhexylphthalate
- HEDTA hydroxyethylethylenediaminetriacetic acid
- glycine phosphorus pentoxide
- tripolyphosphoric acid glycine
- phosphorus pentoxide tripolyphosphoric acid
- the aluminum electrode plate for an electrolytic capacitor to which the present invention is applied is used as an anode of an aluminum electrolytic capacitor in which a functional polymer is used as an electrolyte. That is, the aluminum electrode plate for electrolytic capacitors to which the present invention is applied is used for an electrolytic capacitor in which a dielectric film is formed on the surface and a functional polymer layer is formed on the dielectric film.
- an aluminum plate for an electrolytic capacitor (etched plate) constituting an anode of an aluminum solid electrolytic capacitor
- an aluminum plate having a thickness of 150 ⁇ m or more is subjected to AC etching in an etching solution to enlarge the surface.
- the aluminum plate has an aluminum purity of 99.98% by mass or more, contains less than 30 ppm of copper, 5 to 50 ppm of iron, and the balance is composed of other inevitable impurities.
- the etching solution contains 0.01 ppm or more of one or more additives (chelating agents) having a chelating action such as DTPA, EDTA, DHEG, HEDTA, glycine, phosphorus pentoxide, and tripolyphosphate. And is blended at a concentration of less than 100 ppm.
- the temperature of the etchant is preferably set to 25 ° C. or lower.
- the etching plate obtained by such a method has an anodized film formed on the surface thereof and is used as an anode of an aluminum solid electrolytic capacitor.
- the aluminum plate is etched to a deep position so that the thickness is 150 ⁇ m or more and the thickness of the etched portion is 150 ⁇ m or more in total on both surfaces. More specifically, the etching is carried out to a deep position so that the etching part is 75 ⁇ m or more, 100 ⁇ m or more, and further 120 ⁇ m or more on one side.
- the aluminum plate is AC-etched in an etching solution in which an additive having a chelating action is blended at a concentration of 0.01 ppm or more and less than 100 ppm, thousands to hundreds of thousands per square millimeter Sponge-like pits can be drilled, and such an etching plate has little dissolution on the surface. Therefore, the aluminum electrode plate (etched plate) for electrolytic capacitors to which the present invention is applied has a high etching magnification and a high capacitance.
- the aluminum purity of the aluminum plate is 99.98% by mass or more, it has high toughness and is easy to handle when manufacturing an electrolytic capacitor. If the aluminum purity is less than the lower limit, the hardness increases, the toughness decreases, and damage such as cracking may occur during handling, which is not preferable.
- the thickness of the aluminum plate subjected to the etching treatment may be various depending on the purpose. For example, a thickness of 150 ⁇ m to 1 mm, usually 300 to 400 ⁇ m is used.
- etching process for the aluminum plate at least an etching process for generating etching pits in the aluminum plate (hereinafter referred to as a first etching process) and an etching process for growing the etching pits (hereinafter referred to as a second etching process).
- etching is performed in an etching solution containing an additive.
- An auxiliary etching process may be performed between the first etching process and the second etching process.
- the first etching step (primary electrolytic treatment)
- AC etching is performed with a low concentration aqueous hydrochloric acid solution.
- a pretreatment it is preferable to remove the surface oxide film from the aluminum plate by degreasing and light etching.
- the low-concentration hydrochloric acid aqueous solution used as an etching solution in the primary electrolytic treatment is, for example, an aqueous solution containing 1.5 to 3.0 mol / liter hydrochloric acid and 0.05 to 0.5 mol / liter sulfuric acid in a ratio of 40 to 55. ° C.
- an AC etching condition an AC waveform having a frequency of 10 to 50 Hz is used.
- the AC waveform a sine waveform, a rectangular waveform, an AC / DC superimposed waveform, or the like can be used.
- the current density at that time is 0.4 to 0.5 A / cm 2 , and according to such etching conditions, a large number of pits can be drilled on the surface of the aluminum plate.
- the etching solution used in this main electrolytic treatment is, for example, in an aqueous solution containing 4 to 7 mol / liter hydrochloric acid and 0.05 to 0.5 mol / liter sulfuric acid as a ratio, and the solution temperature is lower than the primary treatment, 25 ° C. or less. The temperature is preferably 15 to 25 ° C.
- an AC etching condition an AC waveform having a frequency of 20 to 60 Hz is used.
- a sine waveform, a rectangular waveform, an AC / DC superimposed waveform, or the like can be used.
- the current density is set to 0.2 to 0.3 A / cm 2 which is lower than that of the primary electrolytic treatment
- the treatment time is set to a time during which treatment can be performed up to a predetermined etching site thickness, and pits drilled by the primary electrolytic treatment are further drilled.
- one or more additives (chelating agents) that chelate such as DTPA, EDTA, DHEG, HEDTA, glycine, phosphorus pentoxide, etc. are added to the etching solution.
- the etching process is performed for about 60 seconds under the conditions of a duty ratio of about 0.7 to 0.9 and a current density of 0.12 to 0.17 A / cm 2 .
- the bulk density of the etched portion is 0.6 to 1.2, and an etched portion having the following pit diameter and number is formed.
- the diameter and number of pits can be measured with an image analyzer. That is, after the etched surface is polished at predetermined intervals in the depth direction, the hole diameter and number of each polished surface are measured with an image analyzer, and by calculating the ratio of the number of pits of 0.01 to 1 ⁇ m ⁇ , The proportion of pits having a specific size diameter in each layer can be measured. By applying the present invention, it can be determined that a large number of pits having a specific size diameter are perforated uniformly with respect to the etching site.
- the total of both surfaces is 150 ⁇ m or more, and at least one surface has an etching site of 75 ⁇ m or more, 100 ⁇ m or more, and further 120 ⁇ m or more in the depth direction from the surface, and 0.01 to
- An aluminum etched plate for electrolytic capacitors in which the number of pits of 1 ⁇ m ⁇ is 70% or more, preferably 75% or more of the total number of pits on each surface can be obtained. If such an aluminum etched plate for electrolytic capacitors is anodized and used as an anode, an electrolytic capacitor having a large capacitance and low ESR can be realized.
- the diameter measured by the image analysis apparatus is set to 0.001 ⁇ m ⁇ or more.
- the total of both surfaces is 150 ⁇ m or more, and at least one side is formed with an etching site of 75 ⁇ m or more, preferably 100 ⁇ m or more, more preferably 120 ⁇ m or more in the depth direction from the surface.
- the thickness of the etching site is less than the above value, it is not possible to expect a reduction in the size of the electrolytic capacitor or a reduction in the number of stacked electrodes in consideration of the capacitance.
- the capacitance will be reduced.
- it is 0.1 ⁇ m ⁇ or less.
- the presence of such sized pits is 70% or more, preferably 75% or more of the total number of pits on each surface, so that an electrolytic capacitor having a high capacitance and a low ESR can be manufactured. More preferably, it is 80% or more.
- the measurement position of the pit size is a position deeper than 20 ⁇ m from the surface because there is dissolution that does not contribute to surface area expansion during electrolytic etching near the surface, and the pit diameter is increased by connecting the pits. Further, since the boundary surface between the etching part and the core part is uneven and is not constant, the etching depth is set to a position 10 ⁇ m shallower from the position (between the etching part and the core part) on the surface.
- the solid electrolyte is not particularly limited and may be a known solid electrolyte.
- polypyrrole, polythiophene, polyaniline and the like can be used.
- the aluminum electrode plate for an electrolytic capacitor to which the present invention is applied has an aluminum purity of 99.98% by mass or more, and the number of Fe-containing intermetallic compounds having a particle size equivalent to a sphere of 0.1 to 1.0 ⁇ m ⁇ is 1 ⁇ 10 7 to 10 10.
- the ratio of the pits of the specific size diameter be increased, but a capacitor with a lower ESR can be produced. This is presumably because the chemical conversion film is formed with a uniform thickness on the pit surface and is easily impregnated with the solid electrolyte because the particle size is small for a large amount of intermetallic compounds.
- the aluminum plate having an aluminum purity of 99.98% by mass or more preferably contains, for example, Fe 5-50 ppm and Cu less than 30 ppm as elements other than Al, Si 60 ppm or less, preferably 40 ppm or less. This is because when Fe and Si exceed the upper limit values, crystallized substances and precipitates of coarse intermetallic compounds containing Fe and Si are generated, and the leakage current increases. In the case of Si, simple Si is also generated, which is not preferable for the same reason. If Cu exceeds the upper limit value, the corrosion potential of the matrix is greatly changed and no good etching may be performed.
- the content of 5 to 50 ppm of Fe is a well-known value such as Al m Fe, Al 6 Fe, Al 3 Fe, Al-Fe-Si, Al- (Fe, M) -Si (M is other This is preferable because an intermetallic compound such as (metal) is generated and tends to be a pit starting point for AC etching. Containing less than 30 ppm of Cu is preferable because the corrosion potential of the matrix can be stabilized in the presence of Fe, and pits of a specific size can be easily formed.
- the preferable content of Cu is 25 ppm or less, and the lower limit is 2 ppm or more, more preferably 3 ppm or more.
- Ni, Ti and Zr are each 10 ppm or less, preferably 3 ppm or less. Further, other impurities are preferably 3 ppm or less. As a result, since the pit starts in the above-described AC etching method, it becomes easy to drill pits having a specific size in a spongy shape.
- Such high-purity aluminum is produced by refining electrolytic primary metal.
- a purification method used at this time a three-layer electrolytic method or a crystal fractionation method is widely employed, and most of elements other than aluminum are removed by these purification methods.
- Fe and Cu since it can be used as a trace alloy element rather than as an impurity, the content of each element after purification is measured, and when the content of Fe and Cu is less than a predetermined amount, during slab casting, The content of Fe or Cu can be adjusted by adding Al-Fe, Al--Cu master alloy or the like into the molten metal.
- an aluminum plate containing 1 ⁇ 10 7 to 10 10 / cm 3 of Fe-containing intermetallic compound having a particle size equivalent to a sphere and having a diameter of 0.01 to 1.0 ⁇ m ⁇ for example, the aluminum purity is 99.98% by mass or more
- a slab was obtained, and then homogenized at a temperature of 530 ° C or higher.
- a hot rolled sheet having a number of passes corresponding to (400 ° C.) of 3 times or more, or 30 minutes or more and 60 minutes or less, which is subjected to etching to a predetermined thickness only by cold rolling.
- an intermetallic compound having a preferred size and containing a predetermined number of Fe can be easily obtained.
- the size and number of intermetallic compounds containing Fe can be measured with an image analyzer.
- the particle size of the intermetallic compound containing Fe is equivalent to a sphere and is less than 0.01 ⁇ m ⁇ , it tends not to be the nucleus of etching pits by a known method. On the other hand, if it exceeds 1.0 ⁇ m ⁇ , the leakage current tends to be affected when the capacitor is assembled. If the number of intermetallic compounds containing Fe with a particle size equivalent to a sphere of 0.01 to 1.0 ⁇ m ⁇ is less than 1 ⁇ 10 7 / cm 3 , the proportion of pits of a specific size is small, and 1 ⁇ 10 10 / cm 3 If it exceeds, excessive dissolution increases.
- an aluminum plate having a thickness of 0.25 mm is obtained by subjecting an aluminum purity of 99.99% by mass or more to slabs containing 15 ppm copper, 30 ppm iron, 40 ppm silicon, and the remainder from other unavoidable impurities, followed by predetermined rolling.
- Second stage etching (second etching process) Etching solution composition: 7 mol / liter hydrochloric acid + 0.5 mol / liter sulfuric acid mixed aqueous solution
- Additive (chelating agent) type as shown in Table 1
- Electrolytic waveform sinusoidal alternating current, frequency 20Hz
- Current density: 0.3A / cm 2 Electricity: 450C / cm 2 AC etching was performed to obtain an etched plate.
- chelating agents DTPA, EDTA,
- Example Nos. 1 to 7 the capacitance compared to Comparative Example 1 (Sample No. 10) in which no additive (chelating agent) is blended. Is improved by 60 to 70%.
- the first stage etching (first etching step) Etching solution composition: 3 mol / liter of hydrochloric acid + 0.5 mol / liter of sulfuric acid mixed solution
- Electrolytic waveform sine wave AC, frequency 50Hz Current density: 0.5A / cm 2 Electricity: 30C / cm 2
- Second stage etching (second etching process) Etching solution composition: 7 mol / liter of hydrochloric acid + 0.5 mol / liter of sulfuric acid mixed aqueous solution
- Electrolytic waveform sinusoidal alternating current, frequency 20Hz Current density: 0.3A / cm 2 Electricity: 450C / cm 2 AC etching was performed to obtain an etched plate.
- 0.01 to 500 ppm of DTPA was added as an additive (chelating agent)
- the etching plate was anodized at a formation voltage of 5 V, and the capacitance was measured.
- Table 2 shows the measurement results of the capacitance.
- the capacitance and the withstand voltage of the film were measured by the methods specified in EIAJ.
- Comparative Example 1 (Sample 10) containing no additive (chelating agent) was used. It can be seen that the capacitance is improved by 60 to 70%.
- Comparative Example 2 (Sample No. 18) containing 500 ppm of DTPA, the capacitance was lower than that of Examples 11 to 17 of the present invention, so the additive amount was less than 100 ppm. To do. That is, the additive (chelating agent) content is 0.01 ppm or more and less than 100 ppm.
- the first stage etching (first etching step) Etching solution composition: 3 mol / liter of hydrochloric acid + 0.5 mol / liter of sulfuric acid mixed solution Etching solution temperature: 40 ° C
- Electrolytic waveform sine wave AC, frequency 50Hz Current density: 0.5A / cm 2 Electricity: 30C / cm 2
- Second stage etching (second etching process) Etching solution composition: 7 mol / liter of hydrochloric acid + 0.5 mol / liter of sulfuric acid mixed aqueous solution
- Electrolytic waveform sine wave AC, frequency 20Hz Current density: 0.3A / cm 2 Electricity: 450C / cm 2 AC etching was performed to obtain an etched plate.
- the temperature of the etching solution used for the second stage etching was changed in the range of 5 to
- Example Nos. 20 to 28 As shown in Table 3, according to Examples 20 to 28 (Sample Nos. 20 to 28) of the present invention containing 0.01 to 90 ppm of DTPA, compared with the Comparative Example (Sample 10) shown in Tables 1 and 2, the static It can be seen that the electric capacity is improved by 60 to 70%.
- Examples 26 to 28 Example Nos. 26 to 28 of the present invention in which the etchant temperature was 30 ° C. or higher
- Examples 20 to 25 (Sample Nos. 20 to 28) of the present invention in which the etchant temperature was 25 ° C. or lower were used. Since the capacitance tends to be lower than that of 25), the etching solution temperature is preferably 25 ° C. or lower.
- the copper content of the aluminum plate was 5 ppm, 15 ppm, 25 ppm, 30 ppm, and 35 ppm. Further, as shown in Table 4, the temperature of the etchant in the second etching step was set to 17 ° C. and 25 ° C.
- the copper content of the aluminum plate should be less than 30 ppm.
- FIG. 1 is a view showing a cross-sectional photograph of an aluminum etched plate for electrolytic capacitors obtained by applying the present invention.
- FIG. 2 is an explanatory diagram when an electrolytic capacitor is manufactured using an anode obtained by anodizing an aluminum etched plate for an electrolytic capacitor to which the present invention is applied.
- an aluminum etched plate 1 for an electrolytic capacitor to which the present invention is applied has etching sites 3 on both sides of a core portion 2.
- the aluminum etched plate 1 for electrolytic capacitors is subjected to, for example, 5V chemical conversion treatment in an aqueous solution of ammonium adipate, and as shown in FIG. 2, the side end face of the aluminum etched plate 1 for electrolytic capacitors is exposed, and the core An anode lead 6 such as a lead wire is joined to the side end face 4 of the portion 2.
- laser welding 5 with a spot diameter reduced to less than the thickness of the core was used. The spot diameter was 20 to 100 ⁇ m ⁇ .
- anodized aluminum etched plate for electrolytic capacitors 1 is impregnated with polypyrrole according to a conventional method to form a functional polymer layer
- the surface of the etched plate on which the functional polymer layer is formed is formed
- a cathode is formed using carbon paste, silver paste, or the like, and, for example, an electrolytic capacitor of 2.5 V / 330 ⁇ F is manufactured.
- an ethanol solution of a pyrrole monomer is dropped into the pit, and ammonium persulfate and an aqueous solution of sodium 2-naphthalenesulfonate are dropped and chemically polymerized to form a precoat layer made of polypyrrole.
- this electrode plate was immersed in an acetonitrile electrolyte containing a pyrrole monomer and sodium 2-naphthalenesulfonate, and a stainless steel wire was brought into contact with a part of the previously formed chemically polymerized polypyrrole layer to serve as an anode, Electrolytic polymerization is performed using a stainless steel plate as a cathode to form an electropolymerized polypyrrole that becomes a functional polymer layer. In addition, it can replace with polypyrrole and can obtain an equivalent characteristic even if it uses polythiophene.
- an aluminum plate is AC-etched in an etching solution containing an additive having a chelating action at a concentration of 0.01 ppm or more and less than 100 ppm, several thousand to several hundred thousand sponges per square millimeter are used.
- the etching plate there is little dissolution on the surface, and the etching proceeds to a depth of 150 ⁇ m or more in total on both sides. More specifically, the etching proceeds to a depth of 75 ⁇ m or more, or 100 ⁇ m or more, and further 120 ⁇ m or more on one side. For this reason, the aluminum electrode plate for electrolytic capacitors with a high etching magnification and a high electrostatic capacity can be obtained.
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Abstract
Description
2 芯部
3 エッチング部位
まず、アルミニウム純度が99.99質量%以上で、銅を15ppm、鉄を30ppm、シリコンを40ppm含有し、残部がその他の不可避不純物からなるスラブから所定の圧延を経て、厚さが0.25mmのアルミニウム板を得た後、このアルミニウム板に以下の条件
1段目エッチング(第1エッチング工程)
エッチング液組成:3モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
エッチング液温度:40℃
電解波形:正弦波交流、周波数50Hz
電流密度:0.5A/cm2
電気量:30C/cm2
2段目エッチング(第2エッチング工程)
エッチング液組成:7モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
添加剤(キレート剤)の種類:表1に示す通り
添加剤(キレート剤)の濃度:30ppm
エッチング液温度:25℃
電解波形:正弦波交流、周波数20Hz
電流密度:0.3A/cm2
電気量:450C/cm2
で交流エッチングを行ない、エッチング板を得た。2段目エッチングに用いるエッチング液には、表1に示すキレート剤(DTPA、EDTA、DHEG、HEDTA、グリシン、5酸化リンおよびトリポリリン酸ソーダ)を配合した。
次に、アルミニウム純度が99.99質量%以上で、銅を15ppm、鉄を30ppm、シリコンを40ppm含有し、残部がその他の不可避不純物からなるスラブから所定の圧延を経て、厚さが0.25mmのアルミニウム板を得た後、このアルミニウム板に以下の条件
1段目エッチング(第1エッチング工程)
エッチング液組成:3モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
エッチング液温度:40℃
電解波形:正弦波交流、周波数50Hz
電流密度:0.5A/cm2
電気量:30C/cm2
2段目エッチング(第2エッチング工程)
エッチング液組成:7モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
添加剤(キレート剤)の種類:DTPA
添加剤(キレート剤)の濃度:表2に示す通り
エッチング液温度:25℃
電解波形:正弦波交流、周波数20Hz
電流密度:0.3A/cm2
電気量:450C/cm2
で交流エッチングを行ない、エッチング板を得た。2段目エッチングに用いるエッチング液には、表2に示すように、添加剤(キレート剤)としてDTPAを0.01~500ppm配合した。
次に、アルミニウム純度が99.99質量%以上で、銅を15ppm、鉄を30ppm、シリコンを40ppm含有し、残部がその他の不可避不純物からなるスラブから所定の圧延を経て、厚さが0.25mmのアルミニウム板を得た後、このアルミニウム板に以下の条件
1段目エッチング(第1エッチング工程)
エッチング液組成:3モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
エッチング液温度:40℃
電解波形:正弦波交流、周波数50Hz
電流密度:0.5A/cm2
電気量:30C/cm2
2段目エッチング(第2エッチング工程)
エッチング液組成:7モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
添加剤(キレート剤)の種類:DTPA
添加剤(キレート剤)の濃度:10ppm
エッチング液温度:表3に示す通り
電解波形:正弦波交流、周波数20Hz
電流密度:0.3A/cm2
電気量:450C/cm2
で交流エッチングを行ない、エッチング板を得た。2段目エッチングに用いるエッチング液の温度について、表3に示すように、5~40℃の範囲で変化させた。
次に、アルミニウム純度が99.99質量%以上で、銅を5~35ppm(表4参照)、鉄を30ppm、シリコンを40ppm含有し、残部がその他の不可避不純物からなるスラブから所定の圧延を経て、厚さが0.25mmのアルミニウム板を得た後、このアルミニウム板に以下の条件
1段目エッチング(第1エッチング工程)
エッチング液組成:3モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
エッチング液温度:40℃
電解波形:正弦波交流、周波数50Hz
電流密度:0.5A/cm2
電気量:30C/cm2
2段目エッチング(第2エッチング工程)
エッチング液組成:7モル/リッタ塩酸+0.5モル/リッタ硫酸の混合水溶液
添加剤(キレート剤)の種類:DTPA
添加剤(キレート剤)の濃度:10ppm
エッチング液温度:25℃、17℃
電解波形:正弦波交流、周波数20Hz
電流密度:0.3A/cm2
電気量:450C/cm2
で交流エッチングを行ない、エッチング板を得た。アルミニウム板の銅含有量については、表4に示すように、5ppm、15ppm、25ppm、30ppm、35ppmとした。また、第2エッチング工程におけるエッチング液の温度については、表4に示すように、17℃、25℃とした。
図1は、本発明を適用して得た電解コンデンサ用アルミニウムエッチド板の断面写真を表す図である。図2は、本発明を適用した電解コンデンサ用アルミニウムエッチド板を陽極酸化して得た陽極を用いて電解コンデンサを製作するときの説明図である。
Claims (4)
- アルミニウム板をエッチング液中で交流エッチングして拡面化する電解コンデンサ用アルミニウム電極板の製造方法において、
前記アルミニウム板は、アルミニウム純度が99.98質量%以上で、銅を30ppm未満、鉄を5~50ppm含有し、残部がその他の不可避不純物からなり、
前記エッチング液には、キレート作用を有する添加剤が0.01ppm以上、かつ、100ppm未満の濃度で配合されていることを特徴とする電解コンデンサ用アルミニウム電極板の製造方法。 - 前記アルミニウム板に対するエッチング工程として、
少なくとも、
前記アルミニウム板にエッチングピットを発生させるエッチング工程と、
前記エッチングピットを成長させるエッチング工程とを行い、
当該エッチングピットを成長させるエッチング工程において、前記添加剤が配合された前記エッチング液中でのエッチングを行なうことを特徴とする請求項1に記載の電解コンデンサ用アルミニウム電極板の製造方法。 - 前記添加剤が配合された前記エッチング液中でのエッチングを行なう際、当該エッチング液の温度を25℃以下に設定することを特徴とする請求項1に記載の電解コンデンサ用アルミニウム電極板の製造方法。
- 前記添加剤は、ジエチレントリアミン5酢酸、エチレンジアミン4酢酸、ジエチルヘキシルフタレート、ヒドロキシエチルエチレンジアミン三酢酸、グリシン、5酸化リンおよびトリポリリン酸塩からなる群から選ばれた1乃至複数のキレート剤であることを特徴とする請求項1乃至3の何れか一項に記載の電解コンデンサ用アルミニウム電極板の製造方法。
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JPH06116757A (ja) * | 1992-10-05 | 1994-04-26 | Sky Alum Co Ltd | 表面欠陥の少ないアルミニウム合金圧延材の製造方法 |
JP2007324252A (ja) * | 2006-05-31 | 2007-12-13 | Nichicon Corp | 電解コンデンサ用電極箔の製造方法 |
JP2008091374A (ja) * | 2006-09-29 | 2008-04-17 | Nichicon Corp | 電解コンデンサ用エッチング箔の製造方法 |
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JPH06116757A (ja) * | 1992-10-05 | 1994-04-26 | Sky Alum Co Ltd | 表面欠陥の少ないアルミニウム合金圧延材の製造方法 |
JP2007324252A (ja) * | 2006-05-31 | 2007-12-13 | Nichicon Corp | 電解コンデンサ用電極箔の製造方法 |
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