JPH01173567A - Alkaline cell - Google Patents

Alkaline cell

Info

Publication number
JPH01173567A
JPH01173567A JP62331222A JP33122287A JPH01173567A JP H01173567 A JPH01173567 A JP H01173567A JP 62331222 A JP62331222 A JP 62331222A JP 33122287 A JP33122287 A JP 33122287A JP H01173567 A JPH01173567 A JP H01173567A
Authority
JP
Japan
Prior art keywords
separator
layer
density
thickness
fiber
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
Application number
JP62331222A
Other languages
Japanese (ja)
Inventor
Kazumasa Yoshida
和正 吉田
Kunio Yoneyama
米山 邦夫
Katsuhiko Fukaya
深谷 克彦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
FDK Twicell Co Ltd
Original Assignee
Toshiba Battery Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Toshiba Battery Co Ltd filed Critical Toshiba Battery Co Ltd
Priority to JP62331222A priority Critical patent/JPH01173567A/en
Publication of JPH01173567A publication Critical patent/JPH01173567A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/44Fibrous material
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/411Organic material
    • H01M50/414Synthetic resins, e.g. thermoplastics or thermosetting resins
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/411Organic material
    • H01M50/429Natural polymers
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M50/00Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
    • H01M50/40Separators; Membranes; Diaphragms; Spacing elements inside cells
    • H01M50/409Separators, membranes or diaphragms characterised by the material
    • H01M50/449Separators, membranes or diaphragms characterised by the material having a layered structure
    • H01M50/457Separators, membranes or diaphragms characterised by the material having a layered structure comprising three or more layers
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Cell Separators (AREA)

Abstract

PURPOSE:To improve the cell performance by using a separator overlappingly constituted of multiple sheets of the integrated paper with a double structure consisting of a layer of beaten natural fibers with increased density and a layer of synthetic fibers. CONSTITUTION:A separator 7 overlappingly constituted of multiple sheets of the integral paper with a double structure consisting of a layer of beaten natural fibers made of alkali-insoluble cotton or pulp and having increased density and a layer of synthetic fibers is used. The separator can be thereby constituted thin, and the cell performance can be improved.

Description

【発明の詳細な説明】 [産業上の利用分野コ この発明はセパレータの構成を改良したアルカリ電池に
関するものである。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to an alkaline battery having an improved separator structure.

[従来の技術] アルカリ電池は重負荷放電に優れ、小形電池では例えば
ストロボやカセットレコーダ等の各種機器においてその
需要がますます増大する傾向lこある。このような背景
のもとに一層小形化並びに高密度化が要求されでいるの
で、セパレータの機能が非常に重要になっている。
[Prior Art] Alkaline batteries are excellent in heavy load discharge, and there is a tendency for demand for small batteries to increase more and more in various devices such as strobes and cassette recorders. Against this background, there is a demand for further miniaturization and higher density, so the function of the separator has become very important.

重負荷放電では電極反応速度を早く行なわせる心安があ
りどのような構成のセパレータを用いるかが大きく影響
するからである。
This is because in heavy load discharge, it is safe to make the electrode reaction speed faster, and the configuration of the separator used has a great influence.

イオン電導性をよくするためには親液性と保液力に優れ
たパルプやレーヨン繊維とビニロンとを混合した混抄紙
からなる有底円筒状のセパレータで通常保液力と強度を
保つために混抄紙を3枚以上貼り合せたものが一般に用
いられていた。
In order to improve ionic conductivity, a cylindrical separator with a bottom is usually used, which is made of pulp or paper mixed with rayon fiber and vinylon, which has excellent lyophilicity and liquid-holding ability, to maintain liquid-holding ability and strength. A paper made of three or more sheets of mixed paper pasted together was commonly used.

従来用いられているセパレータは繊維の太さが10μm
程度のもので構成された不織布で、不織布のおよその密
度は0.2g/cc程度の比較的荒い繊維がからまって
できている。厚さは約140〜180+m程度のものを
3〜4枚重ねて有底円筒状のセパレータを構成している
The fiber thickness of conventionally used separators is 10 μm.
The nonwoven fabric is made up of entangled relatively rough fibers with an approximate density of about 0.2 g/cc. The separator has a thickness of about 140 to 180+ m and is stacked in three to four layers to form a cylindrical separator with a bottom.

このセパレータが電解液と接解すると十分に液を含浸し
それぞれの繊維が膨潤するため、セパレーター枚の厚さ
は200μm程度になり3枚を重ねたセパレータでは6
00Pm程度に膨潤する。
When this separator is fused with an electrolytic solution, it is sufficiently impregnated with the liquid and each fiber swells, so the thickness of the separator sheet is about 200 μm, and in the case of a stack of 3 separators, the thickness of the separator sheet is about 200 μm.
It swells to about 00Pm.

これにより、正極と負極の電極間距離が拡大するので短
絡電流値が低下し、したがって連続発光が必要なストロ
ボに用いる場合には必要な特性を十分得られない問題が
あった。
As a result, the distance between the positive and negative electrodes increases, resulting in a decrease in short-circuit current value.Therefore, when used in a strobe that requires continuous light emission, there is a problem in that the required characteristics cannot be obtained sufficiently.

そこで、短絡電流値やストロボ用途に十分なように、セ
パレータを薄く 形成しあるいは二重巻き三重巻きにす
ると、長期間貯蔵した場合に電池の開路電圧が低下する
という問題があった。
Therefore, if the separator was made thin enough or double-wound and triple-wound to be sufficient for short-circuit current and strobe use, there was a problem that the open circuit voltage of the battery would drop when stored for a long period of time.

[発明が解決しようとする問題点コ ーh記のように従来のアルカリ電池においてはセパレー
タが適切なものでないため十分な特性が得られず開路電
圧が低下する等の問題があった。
[Problems to be Solved by the Invention] As described in section 5, in conventional alkaline batteries, the separator is not suitable, so sufficient characteristics cannot be obtained and there are problems such as a decrease in open circuit voltage.

この発明は上記の問題点を解決するためになされたもの
で十分な放電特性が得られ信頼性の高いアルカリ電池を
提供することを目的としている。
The present invention was made to solve the above-mentioned problems, and an object of the present invention is to provide an alkaline battery with sufficient discharge characteristics and high reliability.

[問題点を解決するための手段および作用]上記の目的
を達成するためこの発明のアルカリ電池は、天然繊維を
叩解し密度を増加させた層と合成繊維の層を有する二重
構造の一体紙を複数枚重ねて構成したセパレータを用い
たことを特徴としている。
[Means and effects for solving the problems] In order to achieve the above object, the alkaline battery of the present invention is made of a dual-structure integrated paper having a layer of beaten natural fibers to increase the density and a layer of synthetic fibers. It is characterized by the use of a separator made up of multiple stacked layers.

このような構成をとると叩解天然繊維側が高密度である
ため従来のものに比してセパレータの厚みを薄(するこ
とができ′電池性能を損なうことがない。また密度の増
加により強度が増加するため作業性が向上する。
With this configuration, since the beaten natural fiber side has a high density, the thickness of the separator can be made thinner than conventional ones, without impairing battery performance.In addition, the increased density increases the strength. This improves work efficiency.

[実施例コ 以下、図面を参照してこの発明の一実施例を説明する。[Example code] Hereinafter, one embodiment of the present invention will be described with reference to the drawings.

添付図面はアルカリマンガン電池として構成したこの発
明の実施例を示すものである。図において1は負極端子
を兼ねるキャップであり集電体2が中央部に抵抗溶接さ
れ、ガスケット3の中心を貫通しさらに負極亜鉛4に挿
入されている。ガスゲット3の材料としてはナイロン6
が用いられている。
The accompanying drawings show an embodiment of the invention configured as an alkaline manganese battery. In the figure, reference numeral 1 denotes a cap that also serves as a negative electrode terminal, and a current collector 2 is resistance welded to the center thereof, passes through the center of a gasket 3, and is further inserted into a negative electrode zinc 4. The material for Gasget 3 is nylon 6.
is used.

負極亜鉛4は約150+mの亜鉛粒を水銀3%でアマル
ガム化したものが電解液中でゲル化剤で分散したもので
ある。5は二酸化マンガンを主体とした正極で、鉄にニ
ッケルメッキを施した正極缶6と接触し電気的に接続さ
れている。
The negative electrode zinc 4 is made by amalgamating zinc grains of about 150+ m with 3% mercury and dispersing them in an electrolytic solution with a gelling agent. Reference numeral 5 denotes a positive electrode mainly made of manganese dioxide, which is in contact with and electrically connected to a positive electrode can 6 made of iron plated with nickel.

正極5の内面には不織布からなるセパレータ7が設けら
れ、負極亜鉛4と正極5の接触を防ぐとともをここのセ
パレータ7には電解液が含浸されることによりイオン電
導度が優れたものとナラている。
A separator 7 made of nonwoven fabric is provided on the inner surface of the positive electrode 5 to prevent contact between the negative electrode zinc 4 and the positive electrode 5, and the separator 7 has excellent ionic conductivity by being impregnated with an electrolyte. It's Nara.

正極缶6の開口部には封口板8が配設され、正極缶6の
開口端をかしめることにより気密かつ液密的に封口され
ている。
A sealing plate 8 is disposed at the opening of the positive electrode can 6, and the opening end of the positive electrode can 6 is caulked to seal the opening in an airtight and liquid-tight manner.

この実施例において用いるセパレータ7は天然繊維であ
るコツトンを叩解機で砕き繊維tO,IPmあるいはそ
れ以下に微細化したものを用いて構成した厚さ約40μ
mの叩解天然繊維の層と0.5デニールのビニロン繊維
からなり密度0.2g/ccの不織布の厚さ60μmの
二層を一体的に構成したもので、このような構成体を二
重になるように円筒状に加工しさらに底部を形成して有
底円筒状のセパレータとしたものである。なお、叩解天
然繊維の最も細いものは、0.01μmに達するものも
ある。
The separator 7 used in this embodiment has a thickness of approximately 40 μm and is made of natural fiber Kotton crushed with a beater and refined into fibers tO, IPm or less.
A layer of beaten natural fiber with a thickness of 60 μm and a layer of a nonwoven fabric with a density of 0.2 g/cc made of vinylon fiber with a density of 0.5 denier are integrally constructed. The separator is processed into a cylindrical shape, and then a bottom is formed to obtain a cylindrical separator with a bottom. Note that some of the finest beaten natural fibers reach 0.01 μm.

また、セパレータ7の正極缶5と接触する側は合成繊維
で耐薬品性に優れたビニロンが位置するように配慮され
ている。
Further, consideration is given to placing vinylon, which is a synthetic fiber and has excellent chemical resistance, on the side of the separator 7 that comes into contact with the positive electrode can 5.

セパレータの内側の天然繊維の層は耐アルカリ性の優れ
たαセルロース95チ以上であるコツトンをパルプの叩
解機で微細化したものを用いて構成しているので、これ
により繊維密度は0.6g/ccに増加し、時には0.
8g/ccにも増加させることができる。なお、叩解し
ない場合の繊維密度は0.13〜0.3g/cc程度ζ
こ過゛ぎない。
The natural fiber layer inside the separator is made of α-cellulose, which has excellent alkali resistance and is made into fine particles using a pulp beater, and has a fiber density of 0.6 g/ cc and sometimes 0.
It can be increased to 8 g/cc. In addition, the fiber density when not beaten is about 0.13 to 0.3 g/ccζ
Not too much.

このような層を片側に有する二重構造の構成体によって
形成したセパレータを用いると、電池製造時電解液と接
触しこの電解液を含浸した後の膨潤度は叩解しない場合
に比較して少ないためセパレータの寸法の変形が少く、
したがって円筒状電池において電池内容積に占めるセパ
レータの膨潤の影響が少いので、正極と負極との間の電
極間距離の寸法が従来のものよりも短くかつ叩解繊維側
が高密度となっているので、従来セパレータトシて三重
に形成していたものが二重で十分機能を果すことが明ら
かとなった。
When using a separator formed from a double-structured structure having such a layer on one side, the degree of swelling after contacting and impregnating with electrolyte during battery manufacturing is less than when it is not beaten. There is little deformation of the separator dimensions,
Therefore, in a cylindrical battery, the effect of swelling of the separator on the internal volume of the battery is small, and the distance between the positive and negative electrodes is shorter than that of conventional batteries, and the beaten fiber side is denser. It has now become clear that the conventional triple separator configuration can function satisfactorily with double separators.

tなみlこ従来の三重のセパレータの場合膨潤度が60
0μm程度であったものが、この実施例の二重のセパレ
ータの場合には240μm程度に薄くできた。
In the case of a conventional triple separator, the degree of swelling is 60.
The thickness of the double separator of this example could be reduced from about 0 μm to about 240 μm.

なお、叩解した天然繊維だけで抄紙したものをセパレー
タとすると、電池製造時に必要な機械的な扱いに適する
厚さたとえば1100p程度にすると繊維密度が高いた
め電池内でのイオン透過が十分でなく内部抵抗が増加す
るので好ましくない。
Note that if a separator is made of paper made from beaten natural fibers, and the thickness is suitable for mechanical handling required during battery manufacturing, for example, about 1100p, the fiber density is high, so ion permeation within the battery is not sufficient and the internal This is undesirable because resistance increases.

この実施例の場合には叩解した天然繊維とビニロンとの
二重構造にしているので一枚の厚さを1100p程度に
した場合に機械的扱いに耐えしかも内部抵抗の増加を抑
制することができる特長がある。
In the case of this example, since it has a double structure of beaten natural fiber and vinylon, when the thickness of one sheet is about 1100p, it can withstand mechanical handling and suppress the increase in internal resistance. It has its features.

参考までに、コツトンの叩解天然繊維からなる40Pm
の層と、1.0デニールのビニロン繊維からなる80+
mの層の2重構造の不織布を有底円筒に加工した2層巻
きのこの発明に右けるセパレータと、比較のため叩解し
ないコツトン繊維30%、10ビニール繊維70%を水
に分散混合し7抄紙とした不織布からなる2重巻き並び
に3重巻きの特性は次の通りである。第1表は40°C
で貯蔵した場合の開路電圧の変化を示し、第2表は製造
後1日経過時の短絡電流の変化を示している。
For reference, 40Pm made of cotton-beaten natural fiber.
80+ layer and 1.0 denier vinylon fiber.
A separator according to the present invention, which is a two-layer winding made by processing a double-structured nonwoven fabric with m layers into a cylinder with a bottom, and for comparison, 30% unbeaten cotton fiber and 70% 10 vinyl fiber were dispersed and mixed in water. The characteristics of the double-wrap and triple-wrap made of paper-made nonwoven fabric are as follows. Table 1 is 40°C
Table 2 shows the change in the short-circuit current when one day has passed since manufacture.

以下余白 第   1   表 ■ 第  2  表 第1表ζこよれば、この発明によるものが従来品に比較
して開路電圧が高い上に変化が少なく、第2表によれば
この発明によるものが従来品に比較して短絡電流が大で
あることが明らかである。
Table 1 ζ Table 2 Table 1 ζ According to this, the product according to the present invention has a higher open circuit voltage and less change than the conventional product, and according to Table 2, the product according to the present invention has a higher open circuit voltage than the conventional product. It is clear that the short circuit current is large compared to the product.

なお、この発明においでコツトンまたはパルプ等の天然
繊維を叩解して高密度化する場合に叩解した繊維による
層の密度は0.4 g / cc以上である必要′があ
り0.8g/cc程度までが適当で、それ以上の密度に
なると電池にした場合のイオン透過が悪くなり電流の低
下を生じる。なおこの層の厚さは40amより薄いとピ
ンホールができるので適当でなく、また100mm以上
になると抵抗値が高くなるので適当でないことが解った
In addition, in this invention, when natural fibers such as cotton or pulp are beaten to obtain a high density, the density of the layer of beaten fibers must be 0.4 g/cc or more, and is about 0.8 g/cc. If the density is higher than that, ion permeation becomes poor when used as a battery, resulting in a decrease in current. It has been found that the thickness of this layer is not appropriate if it is thinner than 40 am because pinholes are formed, and if it is more than 100 mm it is not appropriate because the resistance value becomes high.

なお、セパレータとして有底円筒体とする際、底部と筒
部と同一材料で構成することが作業効率上望ましいが、
底部は電池反応を行なう場所でないため、絶縁性を主体
とした材料例えばポリエチレンシート等を用いてもよい
In addition, when using a cylinder with a bottom as a separator, it is desirable for the bottom and the cylinder to be made of the same material in terms of work efficiency.
Since the bottom part is not a place where a battery reaction takes place, a material mainly having insulating properties, such as a polyethylene sheet, may be used.

また合成繊維としてはビニロンが適当であるが、他に耐
アルカリ性Iこ強いポリプロピレン、ポリエチレンある
いはナイロン等も用いることができる。
Vinylon is suitable as the synthetic fiber, but polypropylene, polyethylene, nylon, etc., which have strong alkali resistance, can also be used.

またこれらの合成繊維の層にコツトンやレーヨン等の天
然繊維またはその鰐導体を混入しても親液性が向上して
効果があるが、その量は50チ以下にすること枦゛貯蔵
信頼性を維持するために望ましい。
Also, mixing natural fibers such as cotton or rayon or their crocodile conductors into the synthetic fiber layer will improve the lyophilic property and be effective, but the amount should be less than 50%.Storage reliability desirable to maintain.

[発明の効果コ この発明によれば叩解により密度を増加させた層と合成
繊維の層よりなる二重構造の一体紙を複数枚重ねてセパ
レータを構成しているため、セパレータを薄く構成でき
るので電池性能を損なうことなく信頼性の高い電池を得
ることができる。
[Effects of the invention] According to this invention, the separator is constructed by stacking multiple sheets of double-structure integral paper consisting of a layer with increased density by beating and a layer of synthetic fibers, so the separator can be constructed thinly. A highly reliable battery can be obtained without impairing battery performance.

また密度の増加とともに一体紙の強度が増加するため作
業性の面でも優れたものとすることができる。
Furthermore, since the strength of the integrated paper increases with the increase in density, it can be made excellent in terms of workability.

【図面の簡単な説明】[Brief explanation of the drawing]

薔÷図はこの発明の一実施例の縦断面図である。 The figure below is a longitudinal cross-sectional view of one embodiment of the present invention.

Claims (4)

【特許請求の範囲】[Claims] (1)天然繊維を叩解し密度を増加させた層と合成繊維
の層よりなる二重構造の一体紙を複数枚重ねることによ
り構成したセパレータを用いたことを特徴とするアルカ
リ電池。
(1) An alkaline battery characterized by using a separator constructed by stacking multiple sheets of double-structure integral paper consisting of a layer of beaten natural fibers with increased density and a layer of synthetic fibers.
(2)天然繊維がアルカリ不溶性のコットンまたはパル
プであることを特徴とする特許請求の範囲第1項記載の
アルカリ電池。
(2) The alkaline battery according to claim 1, wherein the natural fiber is alkali-insoluble cotton or pulp.
(3)合成繊維の層はビニロンが50%以上含んだもの
であることを特徴とする特許請求の範囲第1項記載のア
ルカリ電池。
(3) The alkaline battery according to claim 1, wherein the synthetic fiber layer contains 50% or more of vinylon.
(4)天然繊維の層は密度が0.4〜0.8g/ccで
厚さが15〜80μm、合成繊維の層は密度が0.18
〜0.3g/ccで厚さが40〜100μmでありかつ
両層の合計厚さが160μm以下であることを特徴とす
る特許請求の範囲第1項または第2項記載のアルカリ電
池。 カリ電池。
(4) The natural fiber layer has a density of 0.4 to 0.8 g/cc and a thickness of 15 to 80 μm, and the synthetic fiber layer has a density of 0.18
3. The alkaline battery according to claim 1 or 2, wherein the alkaline battery has a thickness of 40 to 100 μm at ~0.3 g/cc, and a total thickness of both layers is 160 μm or less. Potash battery.
JP62331222A 1987-12-26 1987-12-26 Alkaline cell Pending JPH01173567A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62331222A JPH01173567A (en) 1987-12-26 1987-12-26 Alkaline cell

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62331222A JPH01173567A (en) 1987-12-26 1987-12-26 Alkaline cell

Publications (1)

Publication Number Publication Date
JPH01173567A true JPH01173567A (en) 1989-07-10

Family

ID=18241260

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62331222A Pending JPH01173567A (en) 1987-12-26 1987-12-26 Alkaline cell

Country Status (1)

Country Link
JP (1) JPH01173567A (en)

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