JPH0752641B2 - Sealed lead acid battery - Google Patents
Sealed lead acid batteryInfo
- Publication number
- JPH0752641B2 JPH0752641B2 JP60060826A JP6082685A JPH0752641B2 JP H0752641 B2 JPH0752641 B2 JP H0752641B2 JP 60060826 A JP60060826 A JP 60060826A JP 6082685 A JP6082685 A JP 6082685A JP H0752641 B2 JPH0752641 B2 JP H0752641B2
- Authority
- JP
- Japan
- Prior art keywords
- mat
- battery
- fiber
- acid battery
- lead acid
- 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.)
- Expired - Fee Related
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M10/00—Secondary cells; Manufacture thereof
- H01M10/06—Lead-acid accumulators
- H01M10/12—Construction or manufacture
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/471—Spacing elements inside cells other than separators, membranes or diaphragms; Manufacturing processes thereof
- H01M50/474—Spacing elements inside cells other than separators, membranes or diaphragms; Manufacturing processes thereof characterised by their position inside the cells
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/471—Spacing elements inside cells other than separators, membranes or diaphragms; Manufacturing processes thereof
- H01M50/477—Spacing elements inside cells other than separators, membranes or diaphragms; Manufacturing processes thereof characterised by their shape
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/471—Spacing elements inside cells other than separators, membranes or diaphragms; Manufacturing processes thereof
- H01M50/48—Spacing elements inside cells other than separators, membranes or diaphragms; Manufacturing processes thereof characterised by the material
- H01M50/483—Inorganic material
-
- 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
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Cell Separators (AREA)
- Secondary Cells (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明は、寿命を延長した密閉型鉛蓄電池に関する。Description: TECHNICAL FIELD The present invention relates to a sealed lead acid battery having an extended life.
(従来の技術) 従来、正、負極板間に密度0.15g/cm3の細繊維マツトを
介在させた極板群の複数群を電槽内に適宜の加圧状態で
不動に収容し、そのマツトに通常の電解液又はコロイド
電解液を含浸保持せしめて成る密閉型鉛蓄電池は公知で
ある。(Prior Art) Conventionally, a plurality of electrode plate groups in which a fine fiber mat having a density of 0.15 g / cm 3 is interposed between positive and negative electrode plates are fixedly housed in a battery case under an appropriate pressure, and A sealed lead-acid battery, in which a mat is impregnated with an ordinary electrolytic solution or a colloidal electrolytic solution and held, is known.
(発明が解決しようとする問題点) 従来の上記蓄電池は、使用中にガラス細繊維マツトの厚
さが収縮して極板との密着性が悪くなり、極板とマツト
との間に間隙を生ずるので電池容量が急激に減少し、寿
命が短かくなることが避けられない。これを防止するた
め、極板群の組み立て時、極めて大きい加圧をかけてマ
ツトを著しく圧縮した状態で極板群を組み立て、この状
態で電槽内に不動に収容することが行なわれているが、
その組み立て並に収容の作業性が悪くなるばかりでな
く、マツトの吸液量が低下し、電解液保持量が著しく少
なくなり容量が不足する場合がある。特に高さの高い大
形電池では、その極板群の上部に液の上昇が少なくな
り、上部では電解液量が特に不足し特性が劣化する等の
不都合を生ずる。(Problems to be Solved by the Invention) In the conventional storage battery described above, the thickness of the glass fine fiber mat shrinks during use, resulting in poor adhesion to the electrode plate, resulting in a gap between the electrode plate and the mat. It is unavoidable that the battery capacity is rapidly reduced and the life is shortened. In order to prevent this, when assembling the electrode plate group, the electrode plate group is assembled in a state in which the mat is remarkably compressed by applying extremely large pressure, and in this state, it is immovably housed in the battery case. But,
Not only the workability of assembling but also the housing is deteriorated, but the liquid absorption amount of the mat is lowered, and the electrolyte holding amount is remarkably reduced, so that the capacity may be insufficient. Particularly in the case of a large battery having a high height, the rise of the liquid is reduced in the upper part of the electrode plate group, and the amount of the electrolytic solution is particularly insufficient in the upper part, and the characteristics are deteriorated.
(問題点を解決するための手段) 本発明は、電解液の含浸によつて厚さが減少して正、負
極板面との密着性が劣化することなく而も高さが大きい
場合でも良好に充分な電解液を長期に亘り保持し、電池
寿命の延長した。更には極板群の組み立て時に従来のよ
うな大きい加圧を必要とせず、組立て並に電槽内への組
込み作業の容易な密閉型鉛蓄電池を提供するもので、繊
維径約15〜50μの範囲から成り且つ密度0.1g/cm3以下の
太繊維マツトを中核としその両面に肉薄の細繊維マツト
を重合して成る複合マツトを、正、負極板間に介在させ
その正、負極板の対向面にその両面の細繊維マツトを密
着させて組み立てた極板群の所望個を電槽内に適宜の加
圧状態で不動に収容すると共にコロイド電解液を複合マ
ツトに含浸保持せしめて成る。(Means for Solving Problems) The present invention is good even when the height is large without decreasing the thickness due to the impregnation of the electrolytic solution, and the adhesion with the positive and negative electrode plate surfaces is deteriorated. In addition, sufficient electrolyte was retained for a long period of time to extend battery life. Furthermore, it provides a sealed lead-acid battery that does not require large pressurization as in the past when assembling the electrode plate group and is easy to assemble and install in the battery case. A composite mat consisting of a thick fiber mat having a density of 0.1 g / cm 3 or less and having a thin fiber mat polymerized on both sides of the core as a core, and a positive and negative electrode plate facing each other with a composite mat interposed between the positive and negative electrode plates. A desired group of electrode plates assembled by closely adhering the fine fiber mats on both sides to the surface is immovably accommodated in a battery case under appropriate pressure and the colloidal electrolyte is impregnated and held in the composite mat.
(実施例) 次に本発明実施例を添付図面につき説明する。(Embodiment) Next, an embodiment of the present invention will be described with reference to the accompanying drawings.
図面は、本発明の密閉型鉛蓄電池の截断側面図を示し、
(1)は正極板、(2)は負極板、(3)は各正極板
(1)と負極板(2)との間に介在した本発明の要部で
ある複合マツトである。該複合マツト(3)は、繊維径
約15〜50μの範囲から成り且つ密度0.1g/cm3以下の太繊
維マツト(3a)を中核としその両面に細繊維マツト(3
b)(3b)を重合して成るものである。複合マツト
(3)は、太繊維マツト(3a)と両細繊維マット(3b)
(3b)とは夫々各別に作成したものを重合して構成して
も、予め抄造などにより1体に重合構成したものでもよ
い。図示の場合は、2枚の正極板(1)と3枚の負極板
(2)とを使用し、その各正極板(1)と負極板(2)
との間に前記複合マツト(3)を重合介在させて複数個
の極板群に組み立てたものを、適宜の加圧状態で電槽
(4)内に不動に収容したものを示す。かくして、各複
合マツト(3)は、その両面の細繊維マツト(3b)(3
b)でその両側の対向する正、負極板(1)(2)の各
対向面に良好に密着せられた状態で正、負極板間に介在
されることとなる。The drawing shows a cutaway side view of the sealed lead-acid battery of the present invention,
(1) is a positive electrode plate, (2) is a negative electrode plate, and (3) is a composite mat which is an essential part of the present invention interposed between each positive electrode plate (1) and the negative electrode plate (2). The composite mat (3) comprises a thick fiber mat (3a) having a fiber diameter in the range of about 15 to 50 μ and a density of 0.1 g / cm 3 or less as a core, and a fine fiber mat (3) on both sides thereof.
b) Polymerized from (3b). The composite mat (3) is a thick fiber mat (3a) and both fine fiber mats (3b).
The (3b) may be formed by polymerizing separately prepared ones, or may be preliminarily polymerized into one body by paper making or the like. In the illustrated case, two positive electrode plates (1) and three negative electrode plates (2) are used, and each positive electrode plate (1) and negative electrode plate (2) are used.
The composite mat (3) is interposed between the two and the assembly is assembled into a plurality of electrode plates, and the assembly is fixedly housed in the battery case (4) under an appropriate pressure. Thus, each composite mat (3) has a fine fiber mat (3b) (3
In b), the positive and negative electrode plates are interposed between the positive and negative electrode plates (1) and (2) facing each other on both sides of the positive and negative electrode plates in good contact with each other.
この電池の各複合マツト(3)の全体にコロイド電解液
を所望量注入含浸保持させる。かくして、特にその中核
の太繊維マツト(3a)は、繊維径15〜50μで密度0.1g/c
m3以下のもので且つ圧縮されない状態にあるので、ゲル
化電解質の収納蓄積庫として役立ち、長期に亘り細繊維
マツト(3b)(3b)への電解液供給を行なうことができ
ると共に従来のような経時的な複合マツト(3)の収縮
もないので、長期に亘り、その両面の細繊維マツト(3
b)(3b)はその対向する正、負極板(1)(2)面と
の良好な密着状態が維持され、電池寿命の延長をもたら
す。又、電池の極板が特に背が高くても、そのコロイド
電解液の含浸保持は、複合マツト(3)全体に均一に行
き亘る。太繊維マツト(3a)、細繊維マツト(3b)は、
折紙法などでつくつた不織布であることが一般で、太繊
維マツト(3a)は、圧縮力に耐え、而もコロイド電解液
を充分に含浸保持できるには、前記の繊維径と低密度が
必要であるが、就中、20〜40μの繊維径の単独又は混合
のものを使用し、密度0.05g/cm3以下が好ましい。細繊
維マツト(3b)は、極板面との密着性、収縮性の観点よ
り、平均繊維径0.1〜5μ程度の細繊維を使用し、特に
厚さ1mm以下好ましくは0.3〜0.6mmとすることにより、
電解液の減少時の収縮による密着性の低下がなく、長期
に亘り極板面との良好な密着性が保持できる。コロイド
電解液は、けい酸ゾル、アルミナゾル、その他のゾル状
物質の単独又は混合物を必要量の希硫酸電解液に混合し
たものを使用し、これを電池内にその複合マツト(3)
に注入含浸せしめゲル化させるか、太繊維マツト(3a)
中に希硫酸でゲル化する微細けい酸粉末などのゲル化物
質粉を分散混入させておき、これに希硫酸を注入するこ
とによりコロイド電解液のゲル化電解質を含有する複合
マツト(3)を得ることができる。A desired amount of colloidal electrolyte is injected and held in the whole of each composite mat (3) of this battery. Thus, in particular, the core thick fiber mat (3a) has a fiber diameter of 15 to 50 μ and a density of 0.1 g / c.
Since it is less than m 3 and is not compressed, it serves as a storage container for the gelled electrolyte, and can supply the electrolytic solution to the fine fiber mats (3b) (3b) for a long period of time, as well as the conventional method. Since there is no contraction of the composite mat (3) over time, the fine fiber mats (3
In b) and (3b), the good contact state with the facing positive and negative electrode plates (1) and (2) is maintained, and the battery life is extended. Even when the electrode plate of the battery is particularly tall, the impregnation and holding of the colloidal electrolyte is evenly distributed over the entire composite mat (3). Thick fiber mat (3a) and fine fiber mat (3b)
Generally, it is a non-woven fabric made by the origami method, etc., and the thick fiber mat (3a) must have the above fiber diameter and low density in order to withstand the compressive force and to sufficiently retain the colloidal electrolyte. However, it is preferable to use fibers having a fiber diameter of 20 to 40 μ, alone or in combination, and having a density of 0.05 g / cm 3 or less. As the fine fiber mat (3b), from the viewpoint of adhesion and contractibility with the electrode plate surface, use fine fibers having an average fiber diameter of about 0.1 to 5 μ, and particularly 1 mm or less, preferably 0.3 to 0.6 mm. Due to
Adhesion does not decrease due to contraction when the electrolyte is reduced, and good adhesion to the electrode plate surface can be maintained for a long period of time. As the colloidal electrolyte, use is made of a mixture of silicic acid sol, alumina sol, and other sol-like substances alone or a mixture with a required amount of dilute sulfuric acid electrolyte, and this is mixed in a battery to form a composite mat (3).
Inject and impregnate into a gel or thick fiber mat (3a)
A powder of a gelling substance such as a fine silicic acid powder that gels with dilute sulfuric acid is dispersed and mixed therein, and dilute sulfuric acid is injected into the powder to form a composite mat (3) containing a gelling electrolyte of a colloidal electrolyte. Obtainable.
図示の電池内蔵の電槽は、常法により電池蓋を施し密閉
型鉛蓄電池とする。次に更に具体例により、従来電池と
の比較試験例により説明する。比較実施例により用いた
共通の電池の諸元は下記表1の通りであつた。The battery case with a built-in battery shown in the figure is a sealed lead-acid battery with a battery lid provided by a conventional method. Next, further specific examples will be described by way of comparative test examples with conventional batteries. The specifications of the common battery used in the comparative examples are shown in Table 1 below.
本発明の電池に使用した複合マツトの太繊維マツトは20
μのガラス繊維にアクリルバインダーを吹き付け密度0.
01g/cm3になるように厚さ4mmに抄造した不織布であり、
細繊維マツトは、平均繊維径1μ、厚さ0.4mmに抄造し
た不織布である。これに前記表1に示すコロイド電解液
量を含浸させて図示の本発明密閉型鉛蓄電池Aを作成し
試験に供した。比較のため、平均繊維径1μ、厚さ4.8m
mの細繊維マツトを作成し、これに同じコロイド電解液
を同量含浸させて密閉型鉛蓄電池Bを作成した。かゝる
各蓄電池A及びBにつき5時間率放電容量試験及び定電
圧過充電寿命試験を行なつた。その結果を下記表2に示
す。 The thick fiber mat of the composite mat used in the battery of the present invention is 20
Acrylic binder is sprayed on glass fiber of μ and density is 0.
It is a non-woven fabric made into paper with a thickness of 4 mm so that it will be 01 g / cm 3 .
The fine fiber mat is a non-woven fabric formed into an average fiber diameter of 1 μ and a thickness of 0.4 mm. This was impregnated with the amount of colloidal electrolyte shown in Table 1 above to prepare a sealed lead-acid battery A of the present invention shown in the figure and used for the test. For comparison, average fiber diameter 1μ, thickness 4.8m
A fine fiber mat of m was prepared and impregnated with the same amount of the same colloidal electrolyte to prepare a sealed lead acid battery B. A 5 hour rate discharge capacity test and a constant voltage overcharge life test were performed for each of the storage batteries A and B. The results are shown in Table 2 below.
上記表2から明らかなように、特に試験電池の様な比較
的高さの高い電池では、上部の電極に対して電解液の供
給の差が容量差となつて現われるものと考えられ、定電
圧過充電においては、極板と電解質との密着性の差が経
時的に現われる結果を示し、本発明電池では、経時的な
電解液の減少に伴なうマツトの厚さが変らないのに対
し、比較電池では電解液減少に伴ないマツトの厚さが減
少することにより寿命に差を生ずるものである。 As is clear from Table 2 above, it is considered that the difference in the supply of the electrolytic solution to the upper electrode appears as a difference in capacity, especially in a battery having a relatively high height such as a test battery, and a constant voltage is considered. In overcharge, shows the result that the difference in adhesion between the electrode plate and the electrolyte appears over time, whereas in the battery of the present invention, the thickness of the mat does not change with the decrease of the electrolytic solution over time. However, in the comparative battery, the life of the battery is varied due to the decrease in the thickness of the mat as the electrolyte decreases.
(発明の効果) このように、本発明によるときは、正、負電極板間に繊
維径約15〜50μの範囲から選択して密度0.1g/cm3以下と
した太繊維マツトを中核としその両面に肉薄の細繊維マ
ツトを重合して成る複合マツトを介在させその両面の細
繊維マツトで正、負極板の対向面に密着させた状態で、
電槽内に不動に収容すると共にその複合マツトにコロイ
ド電解液を含浸保持せしめた密閉型鉛蓄電池を構成した
ので、その使用中に、複合マツトの厚さの減少が防止さ
れ、長期に亘りその電解液含浸の両面の細繊維マツトを
対向極板面に良好に密着保持することができ、而もその
中核の太繊維マツトは圧縮されずに多量のコロイド電解
液を均一に貯蔵保持でき、細繊維マツトへの電解液の供
給源として作用し長期寿命の蓄電池をもたらす等の効果
を有する。(Effect of the invention) As described above, according to the present invention, a thick fiber mat having a density of 0.1 g / cm 3 or less selected from the range of the fiber diameter of about 15 to 50 μ between the positive and negative electrode plates is used as the core. In a state where a composite mat formed by polymerizing thin thin fiber mats is interposed on both sides and the thin fiber mats on both sides are in close contact with the positive and negative electrode plates,
Since a sealed lead-acid battery was constructed in which the colloidal electrolyte was impregnated and held in the battery case immovably, the thickness of the compound mat was prevented from decreasing during its use, and The fine fiber mats on both sides impregnated with the electrolytic solution can be held in good contact with the opposite electrode plate surface, and the core thick fiber mat can be uniformly stored and held with a large amount of colloidal electrolytic solution without being compressed. It acts as a supply source of the electrolytic solution to the fiber mat and has the effect of providing a storage battery with a long life.
図面は、本発明の実施の1例の密閉型鉛蓄電池の要部の
截断側面図を示す。 (1)……正極板、(2)……負極板、(3)……複合
マツト (3a)……太繊維マツト、(3b)(3b)……細繊維マツ
ト (4)……電槽、A……本発明蓄電池The drawings show a cut-away side view of the essential parts of a sealed lead-acid battery according to an embodiment of the present invention. (1) …… positive electrode plate, (2) …… negative electrode plate, (3) …… composite mat (3a) …… thick fiber mat, (3b) (3b) …… thin fiber mat (4) …… battery case , A ... Storage battery of the present invention
Claims (3)
0.1g/cm3以下の太繊維マツトを中核としその両面に肉薄
の細繊維マツトを重合して成る複合マツトを、正、負極
板間に介在させその正、負極板の対向面にその両面の細
繊維マツトを密着させて組み立てた極板群の所望個を電
槽内に適宜の加圧状態で不動に収容すると共にコロイド
電解液を複合マツトに含浸保護せしめて成る密閉型鉛蓄
電池。1. A fiber diameter ranging from about 15 to 50 μm and having a density
A composite mat composed of a thick fiber mat of 0.1 g / cm 3 or less as a core and thin thin fiber mats superposed on both sides of the mat is inserted between the positive and negative electrode plates, and the positive and negative electrodes are opposite to each other. A sealed lead acid battery in which a desired number of electrode plates assembled by closely adhering fine fiber mats are immovably accommodated in a battery case under appropriate pressure and a composite mat is impregnated and protected.
ら成り、且つ厚さ1mm以下である特許請求の範囲(1)
に記載の鉛蓄電池。2. A fine fiber mat having an average fiber diameter of 0.1 to 5 μm and a thickness of 1 mm or less.
Lead acid battery described in.
40μで、密度0.05g/cm3、厚さ4mm程度である特許請求の
範囲(1)に記載の鉛蓄電池。3. The thick fiber mat preferably has a fiber diameter of 20 to
The lead acid battery according to claim (1), which has a density of 0.05 g / cm 3 and a thickness of about 4 mm at 40 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60060826A JPH0752641B2 (en) | 1985-03-27 | 1985-03-27 | Sealed lead acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60060826A JPH0752641B2 (en) | 1985-03-27 | 1985-03-27 | Sealed lead acid battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61224261A JPS61224261A (en) | 1986-10-04 |
JPH0752641B2 true JPH0752641B2 (en) | 1995-06-05 |
Family
ID=13153542
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60060826A Expired - Fee Related JPH0752641B2 (en) | 1985-03-27 | 1985-03-27 | Sealed lead acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0752641B2 (en) |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4137377A (en) * | 1977-10-19 | 1979-01-30 | The Gates Rubber Company | Maintenance-free lead-acid cell |
JPS56138862A (en) * | 1981-02-23 | 1981-10-29 | Yuasa Battery Co Ltd | Nonmaintenance type lead battery |
JPS603741A (en) * | 1983-06-22 | 1985-01-10 | Toshiba Corp | Voice reporting system |
-
1985
- 1985-03-27 JP JP60060826A patent/JPH0752641B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPS61224261A (en) | 1986-10-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4622611A (en) | Double layer capacitors | |
GB1139082A (en) | Gas-tight lead accumulator | |
EP0156292A2 (en) | Electrical double layer capacitor and production of the same | |
EP0377828B1 (en) | Sealed lead-acid battery | |
US4150199A (en) | Precursor for an electrical storage lead battery | |
JPH0752641B2 (en) | Sealed lead acid battery | |
JP2855669B2 (en) | Sealed lead-acid battery | |
JPH0675406B2 (en) | Sealed lead acid battery | |
JPH0794206A (en) | Sealed type lead-acid battery | |
JPS5882472A (en) | Lead storage battery and manufacture thereof | |
JP2862178B2 (en) | Sealed lead-acid battery | |
JP2588631Y2 (en) | Sealed lead-acid battery | |
JPS62136751A (en) | Glass mat for hermetically sealed lead storage battery | |
JPS601757A (en) | Manufacture of sealed lead storage battery | |
JP2794588B2 (en) | Sealed lead-acid battery | |
JP2581237B2 (en) | Manufacturing method of sealed lead-acid battery | |
JPS62223988A (en) | Sealed lead-acid battery | |
JPS6445069A (en) | Sealed lead-acid battery | |
JP2855677B2 (en) | Sealed lead-acid battery | |
JP2571063B2 (en) | Manufacturing method of sealed lead-acid battery | |
JP2533418B2 (en) | Sealed lead acid battery | |
JPS6116469A (en) | Enclosed lead storage battery | |
JPS5749168A (en) | Alkaline cell | |
JP2571064B2 (en) | Sealed lead-acid battery | |
JPH0140471B2 (en) |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |