JPS63110622A - Polarizing electrode - Google Patents
Polarizing electrodeInfo
- Publication number
- JPS63110622A JPS63110622A JP61256002A JP25600286A JPS63110622A JP S63110622 A JPS63110622 A JP S63110622A JP 61256002 A JP61256002 A JP 61256002A JP 25600286 A JP25600286 A JP 25600286A JP S63110622 A JPS63110622 A JP S63110622A
- Authority
- JP
- Japan
- Prior art keywords
- activated carbon
- polarizable electrode
- capacitor
- polarizable
- double layer
- 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.)
- Pending
Links
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 21
- 239000005011 phenolic resin Substances 0.000 claims description 8
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- 229920001568 phenolic resin Polymers 0.000 claims description 5
- 230000003213 activating effect Effects 0.000 claims description 3
- 238000010000 carbonizing Methods 0.000 claims description 3
- 239000011164 primary particle Substances 0.000 claims description 3
- 239000003990 capacitor Substances 0.000 description 14
- 239000012535 impurity Substances 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- -1 polyethylene Polymers 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 238000007750 plasma spraying Methods 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- RXPRRQLKFXBCSJ-GIVPXCGWSA-N vincamine Chemical compound C1=CC=C2C(CCN3CCC4)=C5[C@@H]3[C@]4(CC)C[C@](O)(C(=O)OC)N5C2=C1 RXPRRQLKFXBCSJ-GIVPXCGWSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/10—Energy storage using batteries
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E60/00—Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
- Y02E60/13—Energy storage using capacitors
Landscapes
- Electric Double-Layer Capacitors Or The Like (AREA)
- Battery Electrode And Active Subsutance (AREA)
- Electrochromic Elements, Electrophoresis, Or Variable Reflection Or Absorption Elements (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、電気二重層キャパシタや電池あるいはエレク
トロクロミックディスプレイに用いる分極性電極に関す
る。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to polarizable electrodes used in electric double layer capacitors, batteries, or electrochromic displays.
従来の技術
この種の分極性電極としては、活性炭粉末をフッ素樹脂
バインダーとともに、集電金属に保持したもの(特開昭
56−93216号公報)や活性炭繊維布の片面にアル
ミニウム、ニッケル等の導電層を形成したもの(特開昭
56−83920号公報)がある。PRIOR TECHNOLOGY This type of polarizable electrode includes one in which activated carbon powder is held together with a fluororesin binder on a current collecting metal (Japanese Patent Laid-Open No. 56-93216), and one in which a conductive material such as aluminum or nickel is used on one side of an activated carbon fiber cloth. There is one in which a layer is formed (Japanese Unexamined Patent Publication No. 83920/1983).
前者の活性炭粉末を用いるものは、活性炭に不純物が含
有されており、また原料に天然木材を用いているためロ
ット間のバラつきが大きく、これを用いたキャパシタの
特性も一定しない。さらに活性炭粉本はその比表面積の
大きさが12oOd19程度であり、単位体積あたりに
蓄えられる二重層エネルギーには限界がある。後者の活
性炭繊維を用いるものは、比表面積が26o orn’
/ gと大きくでき、また不純物も少なく電気二重層キ
ャパシタに適しているが、活性炭粉末と比較すると大変
高価であり、加圧しないと空隙率が90%以上占めてお
!7(加圧しても60%以上占める)、空間部分のロス
が大きい。以上のように空間部分が多いため、繊維−本
どうしの接触が少なく、接触抵抗が大きくなる。The former type, which uses activated carbon powder, contains impurities in the activated carbon and uses natural wood as a raw material, so there is large variation between lots, and the characteristics of capacitors using this are also inconsistent. Furthermore, activated carbon powder has a specific surface area of about 120Od19, and there is a limit to the double layer energy that can be stored per unit volume. The latter, which uses activated carbon fibers, has a specific surface area of 26°
/g, and has few impurities, making it suitable for electric double layer capacitors, but it is very expensive compared to activated carbon powder, and if it is not pressurized, it has a porosity of over 90%! 7 (occupies more than 60% even if pressurized), loss of space is large. As described above, since there are many spaces, there is little contact between the fibers and the book, and the contact resistance increases.
発明が解決しようとする問題点
上記のような構成の分極性電極は、活性炭の場合、純度
が低く、また比表面積も十分大きくなく、活性炭繊維の
場合空間助出が低く高wiである。Problems to be Solved by the Invention In the case of a polarizable electrode having the above structure, the purity is low and the specific surface area is not large enough in the case of activated carbon, and the space contribution is low and high wi in the case of activated carbon fiber.
問題点?解決するための手段
本発明は、上記問題点全解決するため、一次粒子径が1
〜2oμmの微粒子状フェノール樹脂を炭化賦活して得
られる活性炭と結合剤により分極性電極を構成するもの
である。problem? Means for Solving The present invention solves all of the above problems by reducing the primary particle diameter to 1.
A polarizable electrode is constituted by activated carbon obtained by carbonizing and activating fine particulate phenol resin of ~20 μm and a binder.
作用
上記の構成により、分極性電極の密度を高め抵抗を低減
しエネルギー密度を高くするとともに、急速充電に適し
、信頼性の高い電気二重層キャパシタを実現することが
できる。ここで用いる微粒子状フェノール樹脂にはたと
えば鐘紡(株)製ペルバール(商品名)がある。このよ
うなフェノール樹脂を炭化賦活して得られる活性炭微粉
末は、従来のやし殻炭等の活性炭粉末(粒径10〜30
0μm程度)と比較すると、粒径が小さく均一であり、
高密度の分極性電極を得ることができる。また極めて不
純物が少なく、比表面積も〜2600d/!jと従来の
ものより2倍以上大きくすることができる。次に結合剤
は、通常のアクリル樹脂やポリエチレンあるいはフッ素
樹脂を用いても良いが、上記フェノール樹脂を熱硬化さ
せて用いると反応性を有するメチロール基により結合力
が強くなり好ましい。Operation With the above configuration, it is possible to increase the density of polarizable electrodes, reduce resistance, and increase energy density, and to realize an electric double layer capacitor that is suitable for rapid charging and has high reliability. The particulate phenolic resin used here includes, for example, Perval (trade name) manufactured by Kanebo Co., Ltd. The activated carbon fine powder obtained by carbonizing and activating such a phenolic resin is a conventional activated carbon powder such as coconut shell charcoal (particle size 10 to 30
(approximately 0 μm), the particle size is small and uniform,
High density polarizable electrodes can be obtained. It also has extremely few impurities and has a specific surface area of ~2600 d/! j can be made more than twice as large as the conventional one. Next, as the binder, ordinary acrylic resin, polyethylene, or fluororesin may be used, but it is preferable to use the above-mentioned phenol resin after thermosetting because the bonding force is strengthened by the reactive methylol group.
実施例 以下本発明の詳細な説明する。Example The present invention will be explained in detail below.
(実施例1)
一次粒子径の1〜20μmの微粒子状フェノール樹脂1
1000°Cの窒素ガス雰囲気下、水蒸気で炭化賦活し
て得られた活性炭と1〜20μmの微粒子状フェノール
樹脂とを重量比で8o : 20で混合し、この混合物
’に3)ン/ cAで加圧成形し、300°Cで加熱し
厚み500μm、i径13m1Dのペレット状とした。(Example 1) Particulate phenolic resin 1 with a primary particle diameter of 1 to 20 μm
Activated carbon obtained by carbonization activation with water vapor in a nitrogen gas atmosphere at 1000°C and fine particulate phenol resin of 1 to 20 μm were mixed at a weight ratio of 8o:20, and this mixture was heated at 3) ton/cA. It was press-molded and heated at 300°C to form pellets with a thickness of 500 μm and an i diameter of 13 m1D.
これの片面に集電体としてアルミニウム層をプラズマ溶
射法によって100μm形成し分極性電極とした。A polarizable electrode was formed by forming a 100 μm aluminum layer as a current collector on one side of this by plasma spraying.
この分極性電極の一対を用いて図に示した扁平型キャパ
シタを構成した。1は分極性電極、2はその集電体を示
す、3は直径16mmのポリプロピレン製多孔膜からな
るセパレータ、4はケース、6は封口板、6はガスケッ
トである。なお電解液には、テトラエチルアンモニウム
のホウフッ化塩全1モル/β溶解したブロビレンカーボ
ネートヲ用いた。A flat capacitor shown in the figure was constructed using this pair of polarizable electrodes. 1 is a polarizable electrode, 2 is a current collector thereof, 3 is a separator made of a polypropylene porous membrane having a diameter of 16 mm, 4 is a case, 6 is a sealing plate, and 6 is a gasket. The electrolytic solution used was brobylene carbonate in which a total of 1 mol/β of tetraethylammonium borofluoride salt was dissolved.
このキャパシタi 2,4 Vで充電後1m人で定電流
放電したところ2.2Fの容量を得た。また70°Cの
雰囲気下で常時2−41f印加したところ、初期容量に
対する1ooo時間後の容量減少率は7%であった。After charging this capacitor with i 2.4 V, a constant current discharge was performed with a 1 m person, and a capacity of 2.2 F was obtained. Further, when 2-41f was constantly applied in an atmosphere of 70°C, the capacity reduction rate after 100 hours with respect to the initial capacity was 7%.
(実施例2)
実施例1と同様な微粒子状活性炭とフッ素樹脂とi80
: 20の重量比で混合後実施例1と同様プレスしペレ
ット状とし同様な大きさ、構成材料を用いてキャパシタ
を作成した。本実施例ではペレット形成時に加熱は行わ
なかった。このキャパシタ全2.4 ”/で充電後1m
Aで定電流放電し、2.15 Fの容量全得た。また7
0’Cの雰囲気下で常時2,4V’i印加したところ、
初期容量に対する1 000時間後の容量減少率は8.
3%であった。(Example 2) Particulate activated carbon, fluororesin, and i80 similar to Example 1
: After mixing at a weight ratio of 20, the mixture was pressed into pellets in the same manner as in Example 1, and a capacitor was produced using the same size and constituent materials. In this example, heating was not performed during pellet formation. This capacitor has a total length of 2.4”/1m after being charged.
A constant current discharge was performed to obtain a total capacity of 2.15 F. Also 7
When 2.4V'i was constantly applied in an atmosphere of 0'C,
The capacity reduction rate after 1000 hours with respect to the initial capacity is 8.
It was 3%.
(実施例3)
実施例1と同様な分極性電極を用い同様な構成のキャパ
シタを作成した。本実施例においては、電解液に10重
量%の速醸溶液を用いた。このキャパシタ’i1.07
で充電後、1mAで定電流放電し、4.1vの容量を得
た。また70’Cの雰囲気下で常時1.□1f印加した
ところ、初期容量に対する1 000時間後の溶量減少
率は9%であった。(Example 3) A capacitor having the same configuration as in Example 1 was created using the same polarizable electrodes. In this example, a 10% by weight quick-brewing solution was used as the electrolyte. This capacitor 'i1.07
After charging, a constant current discharge of 1 mA was performed to obtain a capacity of 4.1 V. Also, under an atmosphere of 70'C, 1. When □1f was applied, the rate of decrease in the amount of melt after 1000 hours was 9% relative to the initial capacity.
(実施例4)
正極側分極性電極として実施例1と同様な電極を用い、
負極としてSnとCdの重量比が85:15の合金(ウ
ッド合金)にリチウムを吸蔵させた非分極性電極を用い
て電気二重層キャパシタを作成した。本実施例において
も他の構成材料は実施例1と同様である。このキャパシ
タは3vの電圧、4.3Fの容量を示した。(Example 4) Using the same electrode as in Example 1 as the positive polarizable electrode,
An electric double layer capacitor was created using, as a negative electrode, a non-polarizable electrode in which lithium was occluded in an alloy (Wood alloy) with a weight ratio of Sn and Cd of 85:15. In this embodiment, other constituent materials are the same as in the first embodiment. This capacitor exhibited a voltage of 3V and a capacitance of 4.3F.
本発明の分極性電極は、上記のような電気二重層キャパ
シタのみならず電池やエレクトロクロミックディスプレ
イ等に広く灰用できる。The polarizable electrode of the present invention can be widely used not only in electric double layer capacitors as described above but also in batteries, electrochromic displays, and the like.
発明の効果
以上のように、本発明によれば従来よりエネルギー密度
の高い、しかも均一で強度の高い分極性電極が得られる
。Effects of the Invention As described above, according to the present invention, it is possible to obtain a polarizable electrode that has a higher energy density than the conventional one, is uniform, and has high strength.
図は本発明の分極性電極を用いた電気二重層キャパシタ
の構成例を示す縦断面図である。
1・・・・・・分極性電極、2・・・・・・集電体、3
・・・・・・セパレータ、4・・・・・・ケース、6・
・・・・・封口板、6・・・・・・ガスケット。
代理人の氏名 弁理士 中 尾 敏 男 ほか1名/−
−−分極、・圧電子
2−−一東盾λイヰく
3−m−でパレーグ
?/4The figure is a longitudinal sectional view showing an example of the structure of an electric double layer capacitor using the polarizable electrode of the present invention. 1... Polarizable electrode, 2... Current collector, 3
... Separator, 4 ... Case, 6.
... Sealing plate, 6... Gasket. Name of agent: Patent attorney Toshio Nakao and 1 other person/-
--Polarization, piezoelectric 2--Ichito shield λ 3-m- and paregu? /4
Claims (2)
樹脂を炭化賦活して得られる活性炭と結合剤より構成し
たことを特徴とする分極性電極。(1) A polarizable electrode comprising activated carbon obtained by carbonizing and activating particulate phenolic resin having a primary particle diameter of 1 to 20 μm and a binder.
1項記載の分極性電極。(2) The polarizable electrode according to claim 1, wherein the binder is a phenolic resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61256002A JPS63110622A (en) | 1986-10-28 | 1986-10-28 | Polarizing electrode |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61256002A JPS63110622A (en) | 1986-10-28 | 1986-10-28 | Polarizing electrode |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS63110622A true JPS63110622A (en) | 1988-05-16 |
Family
ID=17286539
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61256002A Pending JPS63110622A (en) | 1986-10-28 | 1986-10-28 | Polarizing electrode |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63110622A (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63151009A (en) * | 1986-12-16 | 1988-06-23 | 太陽誘電株式会社 | Electric double-layer capacitor |
JPS63153809A (en) * | 1986-12-18 | 1988-06-27 | 旭硝子株式会社 | Electric double-layer capacitor |
JPH03192714A (en) * | 1989-12-22 | 1991-08-22 | Nec Corp | Manufacture of electric double-layer capacitor |
JPH04142017A (en) * | 1990-10-02 | 1992-05-15 | Osaka Titanium Co Ltd | Electric double-layred battery |
JPH053047A (en) * | 1991-02-21 | 1993-01-08 | Osaka Titanium Co Ltd | Electric double layer cell |
JPH05211111A (en) * | 1991-11-20 | 1993-08-20 | Nec Corp | Electric double layer capacitor |
US5603867A (en) * | 1994-09-09 | 1997-02-18 | Nippon Sanso Corporation | Method of production for active carbon electrode for use as electrical double layer condenser and active carbon electrode obtained thereby |
JPWO2010150534A1 (en) * | 2009-06-23 | 2012-12-06 | クラレケミカル株式会社 | Liquid-permeable capacitor, deionized water production method, and deionized water production apparatus |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5024190A (en) * | 1973-02-23 | 1975-03-15 | ||
JPS6027113A (en) * | 1983-07-22 | 1985-02-12 | 松下電器産業株式会社 | Electric double layer capacitor |
JPS60170172A (en) * | 1984-02-13 | 1985-09-03 | Matsushita Electric Ind Co Ltd | Rechargeable electrochemical device |
-
1986
- 1986-10-28 JP JP61256002A patent/JPS63110622A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5024190A (en) * | 1973-02-23 | 1975-03-15 | ||
JPS6027113A (en) * | 1983-07-22 | 1985-02-12 | 松下電器産業株式会社 | Electric double layer capacitor |
JPS60170172A (en) * | 1984-02-13 | 1985-09-03 | Matsushita Electric Ind Co Ltd | Rechargeable electrochemical device |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63151009A (en) * | 1986-12-16 | 1988-06-23 | 太陽誘電株式会社 | Electric double-layer capacitor |
JPS63153809A (en) * | 1986-12-18 | 1988-06-27 | 旭硝子株式会社 | Electric double-layer capacitor |
JPH03192714A (en) * | 1989-12-22 | 1991-08-22 | Nec Corp | Manufacture of electric double-layer capacitor |
JPH04142017A (en) * | 1990-10-02 | 1992-05-15 | Osaka Titanium Co Ltd | Electric double-layred battery |
JPH053047A (en) * | 1991-02-21 | 1993-01-08 | Osaka Titanium Co Ltd | Electric double layer cell |
JPH05211111A (en) * | 1991-11-20 | 1993-08-20 | Nec Corp | Electric double layer capacitor |
US5603867A (en) * | 1994-09-09 | 1997-02-18 | Nippon Sanso Corporation | Method of production for active carbon electrode for use as electrical double layer condenser and active carbon electrode obtained thereby |
JPWO2010150534A1 (en) * | 2009-06-23 | 2012-12-06 | クラレケミカル株式会社 | Liquid-permeable capacitor, deionized water production method, and deionized water production apparatus |
JP5687620B2 (en) * | 2009-06-23 | 2015-03-18 | クラレケミカル株式会社 | Liquid-permeable capacitor, deionized water production method, and deionized water production apparatus |
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