JP4278358B2 - Lattice substrate for lead acid battery - Google Patents

Lattice substrate for lead acid battery Download PDF

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Publication number
JP4278358B2
JP4278358B2 JP2002304286A JP2002304286A JP4278358B2 JP 4278358 B2 JP4278358 B2 JP 4278358B2 JP 2002304286 A JP2002304286 A JP 2002304286A JP 2002304286 A JP2002304286 A JP 2002304286A JP 4278358 B2 JP4278358 B2 JP 4278358B2
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Japan
Prior art keywords
substrate
lattice
lead
grid
mass
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Expired - Fee Related
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JP2002304286A
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Japanese (ja)
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JP2004139870A (en
Inventor
淳 古川
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Furukawa Battery Co Ltd
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Furukawa Battery Co Ltd
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Priority to JP2002304286A priority Critical patent/JP4278358B2/en
Application filed by Furukawa Battery Co Ltd filed Critical Furukawa Battery Co Ltd
Priority to PCT/JP2003/004769 priority patent/WO2003088385A1/en
Priority to AU2003227501A priority patent/AU2003227501B8/en
Priority to CNB038007053A priority patent/CN100499227C/en
Priority to DE60324407T priority patent/DE60324407D1/en
Priority to KR1020047000727A priority patent/KR100566624B1/en
Priority to EP03717588A priority patent/EP1496556B1/en
Priority to US10/754,111 priority patent/US7862931B2/en
Publication of JP2004139870A publication Critical patent/JP2004139870A/en
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    • 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

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Description

【0001】
【発明の属する技術分野】
本発明は、鉛蓄電池の格子基板およびそれを用いた鉛蓄電池に関するものである。
【0002】
【従来の技術】
鉛蓄電池は、鉛合金からなる格子基板を用い、これにペースト状の活物質を塗布充填した正負極板をセパレータを介して交互に積層した極板群を電槽に収納し、これに希硫酸からなる電解液を注液して製造されている。
これら鉛蓄電池においては、正極に用いられる格子基板が寿命に左右すると言われており、耐食性と機械的強度の優れたものが要求されている。しかしながら、従来公知の鉛合金では何れも十分とは言えず、その為格子基板の厚みを厚くすることにより、腐食による格子断面積の減少とそれに伴う機械的強度の低下を補う格子基板設計がなされていた。また、格子基板に斜め格子を設けて格子基板の伸びを抑制すること(特許文献1参照)や、耳から遠い側の内骨の縦格子断面積を増やして格子基板の伸びによる損傷を防止すること(特許文献2参照)が提案されているが、いずれもその効果は限定的であり満足の行くものではない。
【0003】
【特許文献1】
特開2001−236963号公報(第2頁右欄の第6行〜第27行、第1図参照)
【特許文献2】
特開2001−266896号公報(第2頁左欄第50行〜右欄第18行、第1図参照)
【0004】
これらの問題を解決すべき、本発明者らは先に全く新しい鉛合金を提案した(特願2002−116593)。この鉛合金はカルシウム0.02質量%以上0.05質量%未満、スズ0.4質量%以上2.5質量%以下、アルミニウム0.005質量%以上0.04質量%以下、バリウム0.002質量%以上0.014質量%以下、残部が鉛と不可避の不純物からなるもの、或いは更にこれらに0.005質量%以上0.07質量%以下の銀、0.01質量%以上0.10質量%以下のビスマス、0.001質量%以上0.05質量%以下のタリウムよりなる群から選ばれた少なくとも一種の元素を含むものである。この合金によれば比重1.280(20℃)の希硫酸中での腐食量も少なく、またクリープ強度も優れたものである。
【0005】
【発明が解決しようとする課題】
鉛蓄電池において長寿命化と軽量化への要求はますます強まっており、行使基板の耐食性と機械的強度を向上させ、かつ格子基板の軽量化を図る必要性に鑑み、本発明者は更に上記合金を用い、格子基板としての伸びに着目し伸びを極力抑制すべく検討し本発明に至ったものである。
【0006】
【課題を解決するための手段】
本発明は、カルシウム0.02質量%以上0.05質量%未満、スズ0.4質量%以上2.5質量%以下、アルミニウム0.005質量%以上0.04質量%以下、バリウム0.002質量%以上0.014質量%以下、残部が鉛と不可避の不純物からなる鉛基合金を用いた格子基板のマス目有効直径(多角形の面積の4倍を多角形の周囲長で除した値)を格子基板厚みの2倍以上としたことを特徴とするものである。
【0007】
【作用】
極板の伸びは基板表面の腐食生成物が蓄電池の充放電に伴い体積変化を起こし、その応力によるクリープ現象で基板自体が伸びるために起こるものと考えられる。基板自体の耐食性は当然のことながら、基板表面に生成する腐食生成物の性質の影響が大きい。即ち、腐食生成物が多孔質であると、電解液の供給が十分であるために充放電が起こり易く、体積変化が顕著となる。その結果、基板の格子表面に新生面が現れて更に腐食が進行する悪循環に陥る。一方腐食生成物が緻密であると電解液が進入しにくいため、充放電が起こりにくく、安定した状態を維持できる。上記した鉛合金は鉛への添加元素の作用により耐食性と共にクリープしにくい性質があり、更に安定な状態を維持できる。従って、従来細かなマス目や太い格子を必要とした正極の格子基板のマス目を粗くし、且つ細くしても伸びにくく、軽量化を図ることが出来る。
【0008】
本発明の格子基板は、重力鋳造や連続鋳造、更には圧延加工後エキスパンドや打抜き加工して得られる。そして特に正極板に用いられることでその効果は顕著であるが、負極板に用いても良い。
【0009】
また、これら格子基板を用いた鉛蓄電池の用途は、自動車用や産業のサイクルユース用(充放電が著しく繰り返し使用されるもの)、スタンバイ用(非常時に備え待機して使用されるもの)として利用され、液式(電槽内に十分に大量の電解液を備えるもの)、シール式(極板群に含浸する程度の電解液を備えるもの)その他巻回式の円筒形電池等あらゆる鉛蓄電池に適用できる。
【0010】
【発明の実施の形態】
0.04%Ca−1.00%Sn−0.020Al−0.008%B−Pb(%は質量%、以下同様)の鉛合金を用いて重力鋳造により図1に示す様に互いに直交する多数の縦格子1と横格子2を枠格子3で囲った厚さ1mmの格子基板を鋳造して得た。4は耳である。格子のマス目の有効直径(多角形の面積の4倍を多角形の周囲長で除した値)を1、2、4.5、6.5、10、15mmと異なる格子基板を多数鋳造した。これら鋳造した格子基板は100℃で1時間熱処理を施し時効硬化させた後公知の正極活物質ペーストを塗布充填した。該活物質ペーストの充填は通常格子基板の縦横格子が露出しない様充填するが、一部が露出する様充填しても良い。次いで活物質ペーストを充填した極板を、温度40℃、湿度95%の雰囲気中で24時間熟成した後乾燥して正極板を得た。これを公知の方法で製造した負極板とポリエチレンセパレータを介して積層して電槽内に収納し、蓋を施し、比重1.2の希硫酸を電解液として注液し電槽化成を行い5時間率容量が40Ahの液式鉛蓄電池を製造した。この鉛蓄電池をJISD5301に定めされた軽負荷寿命に準じ、周囲温度75℃で充放電を1000回行った。その後鉛蓄電池を解体し、正極板を取り出して格子基板の伸びを測定した。
【0011】
比較のために、従来公知の0.60%Ca−1.00%Sn−0.020%Al−Pbの合金を用い同様にして厚さ1mmの格子基板をその有効直径を同様に種種変えて鋳造し、これを正極に用いて液式の鉛蓄電池を製造し、同様にJISD5301に準じ周囲温度75℃で1000回充放電を繰り返した後解体して正極板の格子基板の伸びを測定した。
【0012】
その結果は図2に示した。縦軸は伸び率、横軸は有効直径を示す。この図から明らかな通り、本発明実施品の格子基板ではいずもの比較品に比し伸び率が低い。また本発明実施品はマス目の有効直径が厚みの2倍から10倍の範囲で伸び率が最も低かった。これは格子基板自体の腐食による伸びが少なく、しかもマス目の有効直径が増加したことで活物質の充放電による膨張収縮の影響が緩和されたためと考えられる。
【0013】
一方、比較品の従来合金を用いた場合では、伸び率が本発明品に比し高く、マス目の有効直径が厚みの2倍以上になると伸びの増加が顕著となった。これはマス目の有効直径の増加による活物質の膨張収縮に対する緩和作用に基板自体の腐食による伸びが大きく勝ったためと考えられる。
【0014】
この結果は、鉛合金の各成分組成をCaは0.02〜0.05%未満、Snは0.4〜2.5%、Alは0.005〜0.04%、Baは0.002〜0.014%の範囲で殆ど変わりは無かった。更に、Agを0.005〜0.07%、Biを0.01〜0.10%、Tlを0.001〜0.05%の範囲で一種又は複数の元素を添加しても結果に殆ど変わりはなく良好な結果が得られた。また、鉛合金中に不可避な不純物が入っていても結果は同様に良好である。
【0015】
以上の通り、本発明品は格子基板の伸びを少なくし得ると共に、従来と同等の伸びで良い場合はマス目の有効直径を格子基板厚みの数倍から十数倍とし得て縦格子や横格子の間隔を粗にし得、その分格子基板の軽量化が図れるものである。
【0016】
なお、マス目の有効直径が格子基板の厚みの1倍とした場合は、基板の質量が相対的に大きくなり、軽量化に対する効果が期待できないので、マス目の有効直径は格子基板厚みの2倍以上が必要である。
【0017】
【発明の効果】
以上の通り、本発明によれば、格子基板の伸びを抑えることでき、しかも軽量化の出来る格子基板を提供し得ると共に、これを鉛蓄電池に用いた場合は、長寿命化と軽量化を両立した鉛蓄電池を提供し得ると言う効果を奏するものである。
【図面の簡単な説明】
【図1】 本発明の実施形態の格子基板の正面図
【図2】 充放電後の格子基板の伸び率特性図
【符号の説明】
1縦格子
2横格子
3枠格子
[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a lattice substrate of a lead storage battery and a lead storage battery using the same.
[0002]
[Prior art]
A lead-acid battery uses a grid substrate made of a lead alloy, and an electrode plate group in which positive and negative plates, which are coated and filled with a paste-like active material, are alternately stacked via a separator, is stored in a battery case, and diluted sulfuric acid is contained therein. It is manufactured by injecting an electrolyte solution consisting of
In these lead storage batteries, it is said that the lattice substrate used for the positive electrode is influenced by the life, and those having excellent corrosion resistance and mechanical strength are required. However, none of the known lead alloys can be said to be sufficient. For this reason, by increasing the thickness of the lattice substrate, a lattice substrate design that compensates for a decrease in the lattice cross-sectional area due to corrosion and a corresponding decrease in mechanical strength is made. It was. In addition, the lattice substrate is provided with an oblique lattice to suppress the elongation of the lattice substrate (see Patent Document 1), and the longitudinal lattice cross-sectional area of the inner bone far from the ear is increased to prevent damage due to the elongation of the lattice substrate. (See Patent Document 2), however, the effects are limited and are not satisfactory.
[0003]
[Patent Document 1]
Japanese Patent Laid-Open No. 2001-236963 (see the right column, page 2, lines 6 to 27, FIG. 1)
[Patent Document 2]
JP 2001-266896 A (see page 2, left column, line 50 to right column, line 18, line 1)
[0004]
In order to solve these problems, the present inventors previously proposed a completely new lead alloy (Japanese Patent Application No. 2002-116593). This lead alloy is calcium 0.02 mass% or more and less than 0.05 mass%, tin 0.4 mass% or more and 2.5 mass% or less, aluminum 0.005 mass% or more and 0.04 mass% or less, barium 0.002 % By mass or more and 0.014% by mass or less, the balance being composed of lead and inevitable impurities, or further 0.005% by mass or more and 0.07% by mass or less of silver, 0.01% by mass or more and 0.10% by mass % Or less of bismuth and 0.001% by mass or more and 0.05% by mass or less of at least one element selected from the group consisting of thallium. According to this alloy, the amount of corrosion in dilute sulfuric acid having a specific gravity of 1.280 (20 ° C.) is small, and the creep strength is also excellent.
[0005]
[Problems to be solved by the invention]
In view of the need to improve the corrosion resistance and mechanical strength of the exercise substrate and to reduce the weight of the lattice substrate, the present inventor has further increased the demand for longer life and lighter weight in lead-acid batteries. Using an alloy, focusing on the elongation as a lattice substrate, the inventors have studied to suppress the elongation as much as possible and have reached the present invention.
[0006]
[Means for Solving the Problems]
In the present invention, calcium is 0.02% by mass or more and less than 0.05% by mass, tin is 0.4% by mass or more and 2.5% by mass or less, aluminum is 0.005% by mass or more and 0.04% by mass or less, and barium is 0.002%. more mass% 0.014 mass% or less, the balance being obtained by dividing the perimeter of a polygon four times the square effective diameter (polygon area of the grating substrate using Runamarimoto alloy of lead and unavoidable impurities (Value) is set to be twice or more of the thickness of the lattice substrate.
[0007]
[Action]
It is considered that the elongation of the electrode plate occurs because the corrosion product on the surface of the substrate undergoes a volume change as the storage battery is charged and discharged, and the substrate itself stretches due to the creep phenomenon caused by the stress. Naturally, the corrosion resistance of the substrate itself is greatly influenced by the properties of the corrosion products generated on the substrate surface. That is, when the corrosion product is porous, the electrolyte solution is sufficiently supplied, so that charge / discharge is likely to occur, and the volume change becomes remarkable. As a result, a new surface appears on the lattice surface of the substrate, and a vicious cycle occurs in which corrosion further proceeds. On the other hand, if the corrosion product is dense, the electrolytic solution is difficult to enter, so that charging / discharging is unlikely to occur and a stable state can be maintained. The above lead alloy has the property of being resistant to creep as well as corrosion resistance by the action of an additive element to lead, and can maintain a more stable state. Therefore, the grid of the positive grid substrate, which has conventionally required a fine grid or a thick grid, is roughened, and even if it is thinned, it is difficult to stretch, and the weight can be reduced.
[0008]
The lattice substrate of the present invention can be obtained by gravity casting, continuous casting, further rolling and punching after rolling. And the effect is remarkable by using especially for a positive electrode plate, but you may use for a negative electrode plate.
[0009]
In addition, the use of lead-acid batteries using these lattice substrates can be used for automotive and industrial cycle use (charging and discharging are repetitively used) and for standby (used in preparation for emergencies). For all types of lead-acid batteries such as liquid type (with a sufficiently large amount of electrolyte in the battery case), seal type (with enough electrolyte to impregnate the electrode plate group), and other wound type cylindrical batteries Applicable.
[0010]
DETAILED DESCRIPTION OF THE INVENTION
0.04% Ca-1.00% Sn-0.020Al-0.008% B a -Pb (% is mass%, the same applies hereinafter) by gravity casting and orthogonal to each other as shown in FIG. It was obtained by casting a 1 mm thick lattice substrate in which a large number of vertical lattices 1 and horizontal lattices 2 were surrounded by a frame lattice 3. 4 is an ear. A large number of lattice substrates having different effective diameters (values obtained by dividing four times the polygonal area by the perimeter of the polygon) as 1, 2, 4.5, 6.5, 10, 15 mm were cast. . These cast lattice substrates were heat-treated at 100 ° C. for 1 hour, age-cured, and then applied and filled with a known positive electrode active material paste. The active material paste is usually filled so that the vertical and horizontal grids of the grid substrate are not exposed, but may be filled so that a part of the grid is exposed. Next, the electrode plate filled with the active material paste was aged in an atmosphere of a temperature of 40 ° C. and a humidity of 95% for 24 hours and then dried to obtain a positive electrode plate. This is laminated with a negative electrode plate manufactured by a known method and a polyethylene separator, accommodated in a battery case, covered, and diluted with sulfuric acid having a specific gravity of 1.2 as an electrolytic solution to form a battery case. A liquid lead-acid battery having a time rate capacity of 40 Ah was manufactured. This lead storage battery was charged and discharged 1000 times at an ambient temperature of 75 ° C. in accordance with the light load life specified in JIS D5301. Thereafter, the lead storage battery was disassembled, the positive electrode plate was taken out, and the elongation of the lattice substrate was measured.
[0011]
For comparison, a conventionally known 0.60% Ca-1.00% Sn-0.020% Al-Pb alloy is used and a 1 mm thick lattice substrate is similarly changed in its effective diameter. A liquid type lead-acid battery was produced by casting and using it as a positive electrode. Similarly, charging and discharging were repeated 1000 times at an ambient temperature of 75 ° C. according to JIS D5301, and then disassembled to measure the elongation of the grid substrate of the positive electrode plate.
[0012]
The results are shown in FIG. The vertical axis represents the elongation and the horizontal axis represents the effective diameter. As is clear from this figure, the lattice substrate of the product of the present invention has a lower elongation than any of the comparative products. Further, the product according to the present invention had the lowest elongation when the effective diameter of the cell was in the range of 2 to 10 times the thickness. This is presumably because the lattice substrate itself has little elongation due to corrosion, and the effective diameter of the grid has increased, so that the effect of expansion and contraction due to charging / discharging of the active material has been alleviated.
[0013]
On the other hand, when the comparative conventional alloy was used, the elongation was higher than that of the product of the present invention, and the increase in elongation became significant when the effective diameter of the squares was more than twice the thickness. This is presumably because the elongation due to corrosion of the substrate itself has greatly overcome the relaxation effect on the expansion and contraction of the active material due to the increase in the effective diameter of the grid.
[0014]
As a result, each component composition of the lead alloy is 0.02 to less than 0.05% for Ca, 0.4 to 2.5% for Sn, 0.005 to 0.04% for Al, and 0.002 for Ba. There was almost no change in the range of -0.014%. Further, even if one or more elements are added in the range of 0.005 to 0.07% Ag, 0.01 to 0.10% Bi, and 0.001 to 0.05% of Tl, almost no results are obtained. There was no change and good results were obtained. Even if inevitable impurities are contained in the lead alloy, the result is similarly good.
[0015]
As described above, the product of the present invention can reduce the elongation of the lattice substrate, and when the elongation equivalent to the conventional one is sufficient, the effective diameter of the grid can be increased from several times to several tens of times the thickness of the lattice substrate, so The lattice spacing can be made coarse, and the weight of the lattice substrate can be reduced accordingly.
[0016]
If the effective diameter of the grid is 1 times the thickness of the lattice substrate, the mass of the substrate becomes relatively large and an effect on weight reduction cannot be expected. More than double is required.
[0017]
【The invention's effect】
As described above, according to the present invention, it is possible to provide a lattice substrate that can suppress the elongation of the lattice substrate and that can be reduced in weight. The effect that it can provide the lead acid battery which was made is produced.
[Brief description of the drawings]
FIG. 1 is a front view of a lattice substrate according to an embodiment of the present invention. FIG. 2 is a graph showing elongation characteristics of the lattice substrate after charging and discharging.
1 vertical grid 2 horizontal grid 3 frame grid

Claims (3)

カルシウム0.02質量%以上0.05質量%未満、スズ0.4質量%以上2.5質量%以下、アルミニウム0.005質量%以上0.04質量%以下、バリウム0.002質量%以上0.014質量%以下、残部が鉛と不可避の不純物からなる鉛基合金からなる格子基板において、該格子基板のマス目の有効直径(多角形の面積の4倍を多角形の周囲長で除した値)が格子基板厚みの2倍以上であることを特徴とする鉛蓄電池用格子基板 Calcium 0.02 to 0.05%, Tin 0.4 to 2.5%, Aluminum 0.005 to 0.04, Barium 0.002 to 0 In a lattice substrate made of lead-based alloy consisting of lead and inevitable impurities, the effective diameter of the lattice of the lattice substrate (4 times the polygonal area divided by the perimeter of the polygon) Value) is at least twice the thickness of the lattice substrate, a lattice substrate for a lead-acid battery . 格子基板のマス目の有効直径が格子基板厚みの2倍以上10倍以下であることを特徴とする請求項1に記載の鉛蓄電池用格子基板。The grid substrate for a lead storage battery according to claim 1, wherein an effective diameter of the grid of the grid substrate is not less than 2 times and not more than 10 times the thickness of the grid substrate. 請求項1乃至2に記載のいずれかの鉛蓄電池用格子基板を用いたことを特徴とする鉛蓄電池。A lead-acid battery using the lead-acid battery grid substrate according to claim 1.
JP2002304286A 2002-04-18 2002-10-18 Lattice substrate for lead acid battery Expired - Fee Related JP4278358B2 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
JP2002304286A JP4278358B2 (en) 2002-10-18 2002-10-18 Lattice substrate for lead acid battery
AU2003227501A AU2003227501B8 (en) 2002-04-18 2003-04-15 Lead-based alloy for lead-acid battery, substrate for lead-acid battery and lead-acid battery
CNB038007053A CN100499227C (en) 2002-04-18 2003-04-15 Lead-based alloy, lead acid battery substrate and lead-acid battery
DE60324407T DE60324407D1 (en) 2002-04-18 2003-04-15 LIBERATION ON A LEAD-BASED BATTERY FOR A STORAGE BATTERY, PLATE FOR A STORAGE BATTERY AND STORAGE BATTERY
PCT/JP2003/004769 WO2003088385A1 (en) 2002-04-18 2003-04-15 Lead-based alloy for lead storage battery, plate for lead storage battery and lead storage battery
KR1020047000727A KR100566624B1 (en) 2002-04-18 2003-04-15 Lead­based alloy for lead storage battery, plate for lead storage battery and lead storage battery
EP03717588A EP1496556B1 (en) 2002-04-18 2003-04-15 Lead-based alloy for lead-acid battery, grid for lead-acid battery and lead-acid batterry
US10/754,111 US7862931B2 (en) 2002-04-18 2004-01-08 Lead-based alloy for lead-acid battery, substrate for lead-acid battery and lead-acid battery

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JP4646572B2 (en) * 2004-08-27 2011-03-09 古河電池株式会社 Positive electrode plate for sealed lead-acid battery and sealed lead-acid battery using the positive electrode plate
JP4868847B2 (en) * 2005-12-23 2012-02-01 古河電池株式会社 Lead acid battery
TR200807567A1 (en) 2008-10-08 2010-04-21 Mutlu Akü Ve Malzemeleri̇ Sanayi̇ Anoni̇m Şi̇rketi̇ An alloy
JP2013122838A (en) * 2011-12-09 2013-06-20 Furukawa Battery Co Ltd:The Positive electrode grid for lead acid battery

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