JP2005044761A - Lattice board for lead-acid battery, and lead-acid battery using it - Google Patents
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- 239000002253 acid Substances 0.000 title claims description 12
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 7
- 239000000956 alloy Substances 0.000 claims abstract description 7
- 229910052788 barium Inorganic materials 0.000 claims abstract description 5
- 229910052797 bismuth Inorganic materials 0.000 claims abstract description 5
- 239000011575 calcium Substances 0.000 claims abstract description 5
- 239000012535 impurity Substances 0.000 claims abstract description 5
- 229910052709 silver Inorganic materials 0.000 claims abstract description 5
- 229910052718 tin Inorganic materials 0.000 claims abstract description 5
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims abstract description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 4
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 claims abstract description 4
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052791 calcium Inorganic materials 0.000 claims abstract description 4
- 239000004332 silver Substances 0.000 claims abstract description 4
- 229910052716 thallium Inorganic materials 0.000 claims abstract description 4
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000000758 substrate Substances 0.000 claims description 50
- 238000003860 storage Methods 0.000 claims description 9
- 230000007797 corrosion Effects 0.000 abstract description 14
- 238000005260 corrosion Methods 0.000 abstract description 14
- 229910000978 Pb alloy Inorganic materials 0.000 abstract description 11
- 239000000203 mixture Substances 0.000 abstract description 2
- 239000013585 weight reducing agent Substances 0.000 abstract description 2
- 206010026865 Mass Diseases 0.000 abstract 1
- 230000002093 peripheral effect Effects 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000011149 active material Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000007599 discharging Methods 0.000 description 4
- 239000008151 electrolyte solution Substances 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000005266 casting Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000007774 positive electrode material Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000004080 punching Methods 0.000 description 1
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- 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
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Abstract
Description
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。 The present invention relates to a lattice substrate of a lead storage battery and a lead storage battery using the same.
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。 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 stored in the battery case. It is manufactured by injecting an electrolyte solution consisting of
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。 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. Therefore, 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.
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2003−147589)。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、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。 In order to solve these problems, the present inventors previously proposed a completely new lead alloy (Japanese Patent Application No. 2003-147589). This lead alloy has a calcium content of 0.02% to less than 0.05%, tin content of 0.4% to 2.5%, barium content of 0.002% to 0.014%, and the balance being lead. Inevitable impurities, or further 0.005% by mass to 0.07% by mass silver, 0.01% by mass to 0.10% by mass bismuth, 0.001% by mass to 0.05% It contains at least one element selected from the group consisting of thallium and less than mass%. 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.
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。 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.
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、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鉛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。 In the present invention, calcium is 0.02 mass% or more and less than 0.05 mass%, tin is 0.4 mass% or more and 2.5 mass% or less, barium is 0.002 mass% or more and 0.014 mass% or less, and the balance is lead. Inevitable impurities, or further 0.005% by mass to 0.07% by mass silver, 0.01% by mass to 0.10% by mass bismuth, 0.001% by mass to 0.05% The grid effective diameter of the lattice substrate using a lead alloy containing at least one element selected from the group consisting of thallium of less than mass% (value obtained by dividing the area of the polygon by 4 times the perimeter of the polygon) It is characterized in that it is at least twice the thickness of the lattice substrate.
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。 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.
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。 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.
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。 In addition, the use of lead-acid batteries using these grid 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.
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。 According to the present invention, it is possible to provide a lattice substrate that can suppress the elongation of the lattice substrate and can be reduced in weight, and when used in a lead storage battery, a lead storage battery that achieves both long life and light weight can be obtained. There is an effect that it can be provided.
0.04%Ca−1.00%Sn−0.008%Bi−残Pb(%は質量%、以下同様)の鉛合金を用いて非酸化状態下で重力鋳造により図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。
As shown in FIG. 1 by gravity casting using non-oxidized lead alloy of 0.04% Ca-1.00% Sn-0.008% Bi-residual Pb (% is mass%, hereinafter the same). It was obtained by casting a 1 mm thick lattice substrate in which a large number of orthogonal
比較のために、従来公知の0.60%Ca−1.00%Sn−0.020Al−残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。 For comparison, a conventionally known 0.60% Ca-1.00% Sn-0.020Al-residual Pb alloy was used to cast a 1 mm-thick lattice substrate in the same manner, while varying its effective diameter. Then, using this as a positive electrode, a liquid type lead-acid battery was manufactured. Similarly, charging and discharging were repeated 1000 times at an ambient temperature of 75 ° C. according to JIS D5301, and then disassembled, and the elongation of the grid substrate of the positive electrode plate was measured.
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。 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.
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。 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.
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%、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。 This result shows that the composition of each component of lead alloy is almost the same in the range of Ca 0.02 to less than 0.05%, Sn 0.4 to 2.5% and Ba 0.002 to 0.014%. There was no. 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.
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。 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.
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。 If the effective diameter of the grid is 1 times the thickness of the grid substrate, the mass of the substrate becomes relatively large and an effect on weight reduction cannot be expected. Therefore, the effective diameter of the grid is 2 times the grid substrate thickness. More than double is required.
1 縦格子
2 横格子
3 枠格子
1
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EP3435457A4 (en) | 2016-08-26 | 2019-06-12 | Hitachi Chemical Company, Ltd. | Lead acid storage battery, forged grid and method for producing same |
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JP2010520607A (en) * | 2007-03-02 | 2010-06-10 | ジョンソン コントロールズ テクノロジー カンパニー | Battery negative grid |
JP7198890B1 (en) | 2021-09-13 | 2023-01-04 | 古河電池株式会社 | lead acid battery |
WO2023037822A1 (en) * | 2021-09-13 | 2023-03-16 | 古河電池株式会社 | Lead storage battery |
JP2023041464A (en) * | 2021-09-13 | 2023-03-24 | 古河電池株式会社 | Lead storage battery |
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