JPH0317957A - Nickel plated unwoven electrode and manufacture thereof - Google Patents
Nickel plated unwoven electrode and manufacture thereofInfo
- Publication number
- JPH0317957A JPH0317957A JP1153202A JP15320289A JPH0317957A JP H0317957 A JPH0317957 A JP H0317957A JP 1153202 A JP1153202 A JP 1153202A JP 15320289 A JP15320289 A JP 15320289A JP H0317957 A JPH0317957 A JP H0317957A
- Authority
- JP
- Japan
- Prior art keywords
- nickel
- epoxy resin
- electrode
- nonwoven fabric
- unwoven
- 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
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 title claims abstract description 48
- 229910052759 nickel Inorganic materials 0.000 title claims abstract description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000000835 fiber Substances 0.000 claims abstract description 35
- 239000003822 epoxy resin Substances 0.000 claims abstract description 19
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 19
- 238000007772 electroless plating Methods 0.000 claims abstract description 5
- 150000001412 amines Chemical class 0.000 claims abstract description 4
- 239000004745 nonwoven fabric Substances 0.000 claims description 23
- 238000000576 coating method Methods 0.000 claims description 8
- 239000011248 coating agent Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- -1 impregnating Substances 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 4
- 238000009991 scouring Methods 0.000 claims description 3
- 150000004982 aromatic amines Chemical class 0.000 claims description 2
- 230000004913 activation Effects 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 claims 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 23
- 238000007747 plating Methods 0.000 abstract description 14
- 239000007772 electrode material Substances 0.000 abstract description 5
- 239000004744 fabric Substances 0.000 abstract 2
- 239000007767 bonding agent Substances 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 239000007787 solid Substances 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000006555 catalytic reaction Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- PIBWKRNGBLPSSY-UHFFFAOYSA-L palladium(II) chloride Chemical compound Cl[Pd]Cl PIBWKRNGBLPSSY-UHFFFAOYSA-L 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 2
- 150000008065 acid anhydrides Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- OJIJEKBXJYRIBZ-UHFFFAOYSA-N cadmium nickel Chemical compound [Ni].[Cd] OJIJEKBXJYRIBZ-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000004800 polyvinyl chloride Substances 0.000 description 2
- 238000004080 punching Methods 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000001119 stannous chloride Substances 0.000 description 2
- 235000011150 stannous chloride Nutrition 0.000 description 2
- IVSZLXZYQVIEFR-UHFFFAOYSA-N 1,3-Dimethylbenzene Natural products CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 1
- FUSNOPLQVRUIIM-UHFFFAOYSA-N 4-amino-2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-n-[3-(trifluoromethyl)phenyl]pyrimidine-5-carboxamide Chemical compound O=C1NC(C)(C)CN1C(N=C1N)=NC=C1C(=O)NC1=CC=CC(C(F)(F)F)=C1 FUSNOPLQVRUIIM-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 229920001007 Nylon 4 Polymers 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- BIVUUOPIAYRCAP-UHFFFAOYSA-N aminoazanium;chloride Chemical compound Cl.NN BIVUUOPIAYRCAP-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229910000377 hydrazine sulfate Inorganic materials 0.000 description 1
- 239000012493 hydrazine sulfate Substances 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 description 1
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003348 petrochemical agent Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 239000004094 surface-active agent Substances 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
Landscapes
- Cell Electrode Carriers And Collectors (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明はニッケルーカドミウムアルカリ電池の電極とし
て用いられるニッケルめっき多孔質不織布電極及びその
製造方法に関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a nickel-plated porous nonwoven fabric electrode used as an electrode for a nickel-cadmium alkaline battery and a method for manufacturing the same.
従来、ニッケルーカドミウムアルカリ電池の!極として
は、多孔ニッケル板と二冫ケル粉末とを一体に焼結した
ものが用いられているが、空孔率が80%程度のものし
か得られず、電池の高容量化が不可能であり、空孔率の
大きいものが要求されーでいる。Traditionally, nickel-cadmium alkaline batteries! The electrode is made by sintering a porous nickel plate and Nijikeru powder, but the porosity is only about 80%, making it impossible to increase the capacity of the battery. Therefore, a material with a high porosity is required.
一方、空孔率の大なる電極材料を得る方法としては、特
公昭38−17554、特開昭49112134、特公
昭61−40721、特開昭61−76686等に示さ
れている様に、有機繊維或は有機発泡体を基材として、
(1)ニッケル粉末を含浸させ焼結,還元したもの、(
2)ニッケルめっき後焼戊,還元するもの、(3)ニッ
ケルめっき後そのまま利用するもの等に分類される。On the other hand, as a method for obtaining an electrode material with a large porosity, as shown in Japanese Patent Publication No. 38-17554, Japanese Patent Publication No. 49112134, Japanese Patent Publication No. 61-40721, Japanese Patent Publication No. 61-76686, organic fibers are used. Or using organic foam as a base material,
(1) Impregnated with nickel powder, sintered and reduced, (
It is classified into 2) those that are fired and reduced after nickel plating, and (3) those that are used as is after nickel plating.
上記(1),(2)はいずれも還元雰囲気中での熱処理
を必要とするため、連続した長尺ロール状の電極が電池
組立の際、工程の連続操業が不可能となり、特殊な用途
にしか使用できないという問題がある。従って、かかる
観点から耐アルカリ性を有する繊維からなる有機繊維不
織布に無電解めっき法によりニッケルを被覆して電極材
料とすることが考えられているが、有機繊維とニッケル
めっきの密着性が悪い、引張り強度が小さい等の欠点が
あり、満足する特性のものが得られない等の欠点がある
。Both (1) and (2) above require heat treatment in a reducing atmosphere, which makes continuous long roll-shaped electrodes impossible to operate continuously during battery assembly, making them difficult to use for special purposes. The problem is that it can only be used. Therefore, from this point of view, it has been considered to coat an organic fiber non-woven fabric made of alkali-resistant fibers with nickel using an electroless plating method to make an electrode material. It has drawbacks such as low strength and the inability to obtain products with satisfactory characteristics.
本発明は、上記従来ニッケル極板の欠点、即ち空孔率が
小さいこと、空孔率を大きくした場合に連続化が不可能
なる点を解決するため鋭意研究を積み重ねた結果、有機
繊維で構虞する繊維集合体即ちカード法,エアレイ法,
スパンポンド法,メルトブ口一法等によって形或する繊
維ウエブにアミン硬化型のエポキシ系樹脂を繊維間結合
剤として適用し、ウエブ構戊maが相互に交差,接触す
る部分及び繊維間表面を接着被覆せしめて形成した不織
布に、無電解ニッケルめっきを施すことによって、該繊
維表面に形成されたエポキシ系樹脂被膜表面に付着する
ニッケルめっきの密着力を高めると共に電極の強度も優
れ、多孔質高容量化が達成された連続操業が可能なる電
極材料を得ることに戊功したものである。The present invention was developed as a result of intensive research to solve the drawbacks of the conventional nickel electrode plates, namely, the low porosity and the impossibility of continuous use when the porosity is increased. Fiber aggregates that may cause problems, such as card method, air lay method,
An amine-curing epoxy resin is applied as an interfiber binder to a fiber web formed by a spun-pond method, a melt-bubbled method, etc., and the parts where the web structure intersects and contacts each other and the interfiber surfaces are bonded. Electroless nickel plating is applied to the coated nonwoven fabric, which increases the adhesion of the nickel plating to the surface of the epoxy resin coating formed on the surface of the fibers, and provides excellent electrode strength. We have succeeded in obtaining an electrode material that can be operated continuously.
上記本発明の構戒に用いられる有機繊維は、耐アルカリ
性であるものが望ましく、ポリオレフイン系,ポリ塩化
ビニル系.ポリアクリロニトリル系.ポリアミド系等を
使用する。かかる繊維を用いて形成する繊維集合体とし
てのウェブはランダムウエブ,クロスウェプ,パラレル
ウエブ等の形態で用いられる他、スパンボンド法.メル
トブロー法.7ラッシュ紡糸法による不織布や、ニード
ルパンチ法,ウオータ二一ドルパンチ法等の繊維交絡手
段によって形成する不織布を使用してもよい。The organic fiber used in the composition of the present invention is preferably alkali-resistant, such as polyolefin, polyvinyl chloride, etc. Polyacrylonitrile type. Use polyamide, etc. Webs as fiber aggregates formed using such fibers can be used in the form of random webs, cross webs, parallel webs, etc., as well as spunbond methods. Melt blow method. A nonwoven fabric formed by the 7 rush spinning method, or a nonwoven fabric formed by a fiber entangling method such as a needle punching method or a water-21 dollar punching method may be used.
また、上記ウエブ・不織布に適用し、繊維間相互を接着
,被覆するアミン硬化型のエポキシ系樹脂としては、ビ
スフェノールA型,ビスフェノールF型,テトラヒド口
キシ7エニールメタン,ポリアルコール型,ポリグリコ
ール型,レゾルシン型,ノポラック型等より選択される
。In addition, amine-curing epoxy resins that can be applied to the above webs and non-woven fabrics to bond and coat the fibers include bisphenol A type, bisphenol F type, tetrahydride-7enylmethane, polyalcohol type, polyglycol type, Selected from resorcinol type, noporac type, etc.
また、該エボキシ系樹脂の硬化剤としては脂肪族アミン
,環状脂肪族アミン,芳香族アミンが望ましく、例えば
N−アミノエチルビペラジン,メタキシレンジアミン,
パラメタンジアミン,4 4′〜ジアミノジ7エニルメ
タン等である。Further, as the curing agent for the epoxy resin, aliphatic amines, cycloaliphatic amines, and aromatic amines are preferable, such as N-aminoethylbiperazine, metaxylene diamine,
These include paramethanediamine, 44'-diaminodi7enylmethane, and the like.
次に本発明に於いてエポキシ系樹脂を用いて有機繊維集
合体を接着,被覆する目的は、形成する不織布の強度を
おおきくし、かつニッケルめっき不織布の密着性を向上
させるためであり、強度を大きくするためのみであれば
、その他の硬化剤、例えば無水フタル酸.無水ピロメリ
ット酸等の酸無水物でもよいが、ニッケルめっきの密着
性を共に向上させるためにはアミン系の硬化剤が適して
いる。Next, in the present invention, the purpose of adhering and covering the organic fiber aggregate using epoxy resin is to increase the strength of the nonwoven fabric to be formed and to improve the adhesion of the nickel-plated nonwoven fabric. Other hardening agents, such as phthalic anhydride, if only for increasing the size. Although acid anhydrides such as pyromellitic anhydride may be used, amine-based curing agents are suitable in order to improve the adhesion of nickel plating.
また、エポキシ系樹脂を繊維間結合剤として使用する方
法又はエポキシ系樹脂を被覆する方法としては、浸漬法
,泡糊法,スプレー法.コーティング法その他いずれの
方法でもよいが、均一に繊維間を結合したり、繊維表面
を均一に被覆するためには、浸漬法が望ましい。Methods of using epoxy resin as an interfiber binder or coating with epoxy resin include dipping method, foam glue method, and spray method. Any method other than the coating method may be used, but the dipping method is preferable in order to uniformly bond the fibers and uniformly coat the fiber surface.
無電解ニッケルめっき工程は、a.界面活性剤による精
練、b.パラジウムによる触媒化、c.メッキの順に行
われる。The electroless nickel plating process consists of a. scouring with surfactants, b. Catalysis with palladium, c. This is done in the order of plating.
b.のパラジウムによる触媒化は、(l)塩化第一スズ
/塩酸水溶液で処理した後、塩化パラジウム/塩酸水溶
液で触媒化する方法、(2)硬化剤のアミノ基を利用し
て塩化パラジウム/塩酸水溶液のみで触媒化する方法等
があるが、(1)による方法が最も密着性が優れている
。b. Catalysis with palladium can be carried out by (l) treating with stannous chloride/hydrochloric acid aqueous solution and then catalyzing with palladium chloride/hydrochloric acid aqueous solution; (2) using palladium chloride/hydrochloric acid aqueous solution using the amino group of the curing agent. Although there are methods of catalyzing the film with only the above method, method (1) has the best adhesion.
無電解ニッケルめっきの還元剤としては、高純度のニッ
ケルを得るために、水利ヒドラジン.硫酸ヒドラジン,
塩化ヒドラジニウム等のヒドラジン誘導体を用いる。As a reducing agent for electroless nickel plating, Iruri hydrazine is used to obtain high purity nickel. hydrazine sulfate,
A hydrazine derivative such as hydrazinium chloride is used.
また、無電解ニッケルめっきに使用する有機繊維不織布
は、連続した長尺のものが簡単に得られ連続工程でエポ
キシ系樹脂の被覆を行うことができ、引続き連続して無
電解ニッケルめっきを行ってもよく、あるいはロール状
に巻き取って染色機を利用してメッキ液を強制的に循環
してメッキを施してもよい。In addition, the organic fiber nonwoven fabric used for electroless nickel plating can be easily obtained in a continuous length and coated with epoxy resin in a continuous process, and then electroless nickel plating can be performed continuously. Alternatively, the material may be wound into a roll and plated by forcibly circulating the plating solution using a dyeing machine.
以下本発明を実施例により詳細に説明する。The present invention will be explained in detail below with reference to Examples.
有機繊維としてナイロン(4),ポリプロピレン(8)
,ポリ塩化ビニル0,ポリアクリロニトリル0をそれぞ
れ単独に使用し、ウエブ形或機例えばカード及びクロス
ラツパー機により各々繊維目付60g/iのクロスウエ
ブを形成する。Nylon (4) and polypropylene (8) as organic fibers
, polyvinyl chloride 0, and polyacrylonitrile 0 were used individually, and a cross web with a fiber basis weight of 60 g/i was formed using a web-forming machine, such as a card and a cross wrapper machine.
次に上記各クロスウエブを下記配合液で満たした浸漬槽
に導入し、浸漬後マングル.脱水装置等により配合液が
繊維100部に対し50部(固形分の重量比)となるよ
うに調整した。Next, each of the above-mentioned cross webs was introduced into a dipping tank filled with the following mixed solution, and after dipping, it was mangled. The blended liquid was adjusted to 50 parts (weight ratio of solid content) to 100 parts of fiber using a dehydrator or the like.
配合液
イ.828タイプエボキシ樹脂
lOO部(エポルジョンEA55:カネボウNSC社製
)ロ.ポリアミド系硬化剤
20部(エポキーH258:三井石油化学社製)ハ
.水
但し、イとロの配合比は固形比を示し、イと口の比を一
定にして水を加え
濃度20%(固形分)とする。Mixed liquid a. 828 type epoxy resin
lOO section (Epolsion EA55: manufactured by Kanebo NSC) b. Polyamide hardener
20 parts (Epokey H258: manufactured by Mitsui Petrochemicals) c. Water However, the blending ratio of A and B indicates the solid ratio, and while keeping the ratio of A and B constant, water is added to make the concentration 20% (solid content).
次に配合液を含浸したウエブは乾燥機に導入し、乾燥,
熱処理を施して第1表に示す様に夫々厚み2 . 5
mm − 2 . 7 trII1,目付90g#の基
材不織布を形成した。Next, the web impregnated with the compounded liquid is introduced into a dryer, dried,
After heat treatment, each layer has a thickness of 2.5 mm as shown in Table 1. 5
mm-2. 7 A base nonwoven fabric having trII1 and a basis weight of 90 g was formed.
第 1 表
比較例l
実施例と各々同一の繊維を用い、同一目付に形或したク
ロスウエブA−Dを下記配合液に浸漬した。Table 1 Comparative Example 1 Cross webs A to D made of the same fibers and shaped to the same basis weight as in the example were immersed in the following blended solution.
配合液
イ.828タイプエポキシ樹脂 1
00部(アデカレジンEP4 100 :旭電化社製)
ロ.酸無水物
85部(アデカハードナEH700:旭電化社製)ハ.
キシローノレ
但し、イと口の配合比は固形比を示す。Mixed liquid a. 828 type epoxy resin 1
00 copies (Adeka Resin EP4 100: manufactured by Asahi Denka Co., Ltd.)
B. acid anhydride
85 copies (ADEKA HARDONA EH700: Asahi Denka Co., Ltd.) c.
However, the blending ratio between A and N indicates the solid ratio.
イとロの比を一定にし、キシロールを加え濃度20%(
固形分)とする。Keeping the ratio of A and B constant, add xylol to a concentration of 20% (
solid content).
浸漬後マングルで配合液が繊維100部に対し50部(
固形分の重量比)となるように調整し、乾燥機に導入し
て乾燥,加熱処理を行い、それぞれ基材不織布A−Dを
形成した。After soaking, mangle the blending liquid to 50 parts per 100 parts of fiber (
The weight ratio of the solid content was adjusted so that the weight ratio of the solid content was adjusted, and the mixture was introduced into a dryer and subjected to drying and heat treatment to form base nonwoven fabrics A to D, respectively.
比較例2
実施例と各々同一の繊維を用い、同一の目付に形或した
クロスウエブA−Dを使用し、軽くニードルパンチ加工
を施して不織布とした。Comparative Example 2 A cross web A-D made of the same fibers and shaped to the same basis weight as in the example was used and lightly needle-punched to obtain a nonwoven fabric.
上記実施例及び比較例1.2で得られた各基材不織布(
巾1mX長さ50m)を染色機のキャリャーに巻き付け
精練剤を循環,水洗し、次に塩化第一スズー・LOgI
Q.塩酸2 0 mQ/Qを含んだ水溶液を循環し、水
洗後塩化パラジウムlg/Q塩酸2 0 tnQ/Qを
含む水溶液を循環させて触媒化を行った。Each base material nonwoven fabric obtained in the above Examples and Comparative Example 1.2 (
1m wide x 50m long) is wrapped around the carrier of the dyeing machine, the scouring agent is circulated, washed with water, and then stannous chloride/LOgI
Q. An aqueous solution containing 20 mQ/Q of hydrochloric acid was circulated, and after washing with water, an aqueous solution containing 1 g/Q of palladium chloride and 20 tnQ/Q of hydrochloric acid was circulated for catalysis.
水洗後硫酸ニッケルL8y/Q.クエン酸ナトIJ ウ
A 1 0 gIQ.水和ヒドラジン50mα/l2.
25%アンモニア水1 0 0 mQ/Qを含む無電解
ニッケルめっき液を80’(!に加温して循環した。1
時間後に循環をやめて水洗,乾燥を実施した。After washing with water, nickel sulfate L8y/Q. Sodium citrate IJ uA 10 gIQ. Hydrated hydrazine 50mα/l2.
An electroless nickel plating solution containing 100 mQ/Q of 25% ammonia water was heated to 80' (!) and circulated.
After a period of time, circulation was stopped, and washing and drying were performed.
この様にして形或した本発明のニッケルめっき不職布電
極は図面に示す如く、不織布電極を構戊するナイロン.
ボリブロピレン等の有機繊維(1)が相互に交差,接触
する部分(2)及び該部分からのびる繊維の表面(3)
をエポキシ系樹脂(4)で接着,被覆され、更に上記エ
ポキシ系樹脂(4)で被覆された繊維表面を無電解めっ
きによるニッケル(5)が強固に付着して連続被覆を形
成している。As shown in the drawings, the nickel-plated non-woven fabric electrode of the present invention formed in this manner is made of nylon that constitutes the non-woven fabric electrode.
The part where organic fibers such as polypropylene (1) intersect and contact each other (2), and the surface of the fibers extending from this part (3)
is adhered and coated with an epoxy resin (4), and nickel (5) is firmly adhered to the surface of the fiber coated with the epoxy resin (4) by electroless plating to form a continuous coating.
また、上記実施例,比較例で得られたニッケルめっき不
織布電極の特性値を測定した結果を第2表に示した。Further, Table 2 shows the results of measuring the characteristic values of the nickel-plated nonwoven fabric electrodes obtained in the above Examples and Comparative Examples.
第
2
表
第2表で明らかなる様にめっきの密着性と不織布の引張
強度のいずれにも優れている実施例A−Dについて、空
孔率と体積抵抗を測定した。Table 2 As is clear from Table 2, the porosity and volume resistance of Examples A to D, which are excellent in both plating adhesion and nonwoven fabric tensile strength, were measured.
尚、空孔率は活物質を含浸させるために必要な厚さ1.
5m+nとして計算したが、実際はそれ以上の空孔率を
有する。Incidentally, the porosity is determined by the thickness required to impregnate the active material.
Although it was calculated as 5m+n, it actually has a porosity higher than that.
測定結果を第3表に示した。The measurement results are shown in Table 3.
第3表 4 には見られない新規な電極材料が得られた。Table 3 4 A new electrode material not seen before was obtained.
(1)・・・有機繊維 (3)・・・繊維表面 (5)・・・ニッケル被膜 (2)・・・交差接触部 (4)・・・エポキシ系樹脂 (1)...Organic fiber (3)...Fiber surface (5)...Nickel coating (2)...Cross contact area (4)...Epoxy resin
Claims (3)
一体に接着被覆してなる基材不織布の表面に、無電解め
っきによるニッケル被膜を形成してなることを特徴とす
るニッケルめっき不織布電極。(1) A nickel-plated nonwoven fabric electrode characterized by forming a nickel coating by electroless plating on the surface of a base nonwoven fabric made by integrally adhering and coating an organic fiber aggregate using an epoxy resin as a binder. .
肪族アミン又は芳香族アミンである請求項1記載のニッ
ケルめっき不織布電極。(2) The nickel-plated nonwoven fabric electrode according to claim 1, wherein the curing agent for the epoxy resin is an aliphatic amine, a cycloaliphatic amine, or an aromatic amine.
付与手段により繊維間相互をエポキシ系樹脂で一体に接
着、被覆して不織布を形成した後、精練、触媒活性化処
理を施し、次に無電解めっき法により、該不織布の繊維
表面を被覆するエポキシ系樹脂表面にニッケル被膜を形
成してなることを特徴とするニッケルめっき不織布電極
の製造方法。(3) After forming a nonwoven fabric by bonding and covering the fibers together with an epoxy resin by applying a binder such as impregnating, coating or spraying the organic fiber aggregate, scouring and catalytic activation treatment are performed, A method for producing a nickel-plated nonwoven fabric electrode, comprising forming a nickel film on the surface of an epoxy resin covering the fiber surface of the nonwoven fabric by electroless plating.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1153202A JPH0317957A (en) | 1989-06-15 | 1989-06-15 | Nickel plated unwoven electrode and manufacture thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1153202A JPH0317957A (en) | 1989-06-15 | 1989-06-15 | Nickel plated unwoven electrode and manufacture thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0317957A true JPH0317957A (en) | 1991-01-25 |
JPH0559550B2 JPH0559550B2 (en) | 1993-08-31 |
Family
ID=15557276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1153202A Granted JPH0317957A (en) | 1989-06-15 | 1989-06-15 | Nickel plated unwoven electrode and manufacture thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0317957A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0686718A1 (en) | 1994-06-09 | 1995-12-13 | Sumitomo Electric Industries, Limited | Unwoven metal fabric and method of manufacturing the same |
JP2005071844A (en) * | 2003-08-26 | 2005-03-17 | Japan Vilene Co Ltd | Current collection material for electrochemical element and battery using this as well as electric double layer capacitor using this |
US7879496B2 (en) | 2006-09-07 | 2011-02-01 | Sumitomo Electric Industries, Ltd. | Battery electrode substrate, battery electrode, and alkaline secondary battery including the same |
CN103985882A (en) * | 2014-05-08 | 2014-08-13 | 大连理工高邮研究院有限公司 | Preparation method of combined web-mode flow battery electrode |
-
1989
- 1989-06-15 JP JP1153202A patent/JPH0317957A/en active Granted
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0686718A1 (en) | 1994-06-09 | 1995-12-13 | Sumitomo Electric Industries, Limited | Unwoven metal fabric and method of manufacturing the same |
JP2005071844A (en) * | 2003-08-26 | 2005-03-17 | Japan Vilene Co Ltd | Current collection material for electrochemical element and battery using this as well as electric double layer capacitor using this |
JP4699686B2 (en) * | 2003-08-26 | 2011-06-15 | 日本バイリーン株式会社 | Current collector for electrochemical device, battery using the same, and electric double layer capacitor using the same |
US7879496B2 (en) | 2006-09-07 | 2011-02-01 | Sumitomo Electric Industries, Ltd. | Battery electrode substrate, battery electrode, and alkaline secondary battery including the same |
CN103985882A (en) * | 2014-05-08 | 2014-08-13 | 大连理工高邮研究院有限公司 | Preparation method of combined web-mode flow battery electrode |
Also Published As
Publication number | Publication date |
---|---|
JPH0559550B2 (en) | 1993-08-31 |
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