JPH0234757Y2 - - Google Patents
Info
- Publication number
- JPH0234757Y2 JPH0234757Y2 JP1986116234U JP11623486U JPH0234757Y2 JP H0234757 Y2 JPH0234757 Y2 JP H0234757Y2 JP 1986116234 U JP1986116234 U JP 1986116234U JP 11623486 U JP11623486 U JP 11623486U JP H0234757 Y2 JPH0234757 Y2 JP H0234757Y2
- Authority
- JP
- Japan
- Prior art keywords
- sulfuric acid
- lead
- battery
- electrolyte
- button
- 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
Links
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 48
- 239000002253 acid Substances 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 229910045601 alloy Inorganic materials 0.000 claims description 3
- 239000000956 alloy Substances 0.000 claims description 3
- 239000008151 electrolyte solution Substances 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000006183 anode active material Substances 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 238000013517 stratification Methods 0.000 description 4
- 239000011149 active material Substances 0.000 description 3
- 238000007599 discharging Methods 0.000 description 3
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 239000006182 cathode active material Substances 0.000 description 2
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 2
- 229910001882 dioxygen Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- KEQXNNJHMWSZHK-UHFFFAOYSA-L 1,3,2,4$l^{2}-dioxathiaplumbetane 2,2-dioxide Chemical compound [Pb+2].[O-]S([O-])(=O)=O KEQXNNJHMWSZHK-UHFFFAOYSA-L 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910000978 Pb alloy Inorganic materials 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052924 anglesite Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000003466 welding Methods 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
- 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
Description
【考案の詳細な説明】
産業上の利用分野
本考案は鉛蓄電池の性能向上に関するものであ
る。[Detailed description of the invention] Industrial application field The present invention relates to improving the performance of lead-acid batteries.
従来技術
一般に、鉛蓄電池用陽極板格子体は単純な格子
構造よりなつている。この鉛格子にペーストを充
填し、熟成、乾燥工程を経て未化板を作成する。
この未化板を希硫酸中で化成し、活物質としての
既化板とする。陽極および陰極既化板をセパレー
タを介して隔離し、極板群を組み立て電池とす
る。未化板および既化板の鉛格子体は、陽極、陰
極の両活物質の保持体となるだけではなく、集電
体としての役割も担つている。Prior Art In general, an anode plate lattice body for a lead-acid battery has a simple lattice structure. This lead grid is filled with paste, and an uncured board is created through aging and drying processes.
This uncured plate is chemically converted in dilute sulfuric acid to obtain a cured plate as an active material. The anode and cathode prepared plates are separated through a separator, and the electrode plate group is assembled to form a battery. The lead lattice bodies of the untreated board and the treated board not only serve as a holder for both the anode and cathode active materials, but also serve as a current collector.
電解液硫酸を含む従来の液式鉛蓄電池では、硫
酸が水よりも重いため水溶液にすると硫酸がより
下方に沈降するため、電池下部の硫酸濃度が高
く、上部では低くなるという成層化現象が起こ
る。この電解液硫酸の成層化による電池上部と下
部の硫酸濃度差を小さくするために放電量に対し
ても充電を115〜130%行い、充電末期に発生する
水素および酸素ガスによつて撹拌を行つている。 In conventional liquid lead-acid batteries that contain sulfuric acid as an electrolyte, sulfuric acid is heavier than water, so when it is made into an aqueous solution, the sulfuric acid settles further down, resulting in a stratification phenomenon in which the sulfuric acid concentration is high at the bottom of the battery and low at the top. . In order to reduce the difference in sulfuric acid concentration between the upper and lower parts of the battery due to the stratification of the electrolyte sulfuric acid, charging is performed at 115 to 130% of the discharge amount, and stirring is performed using hydrogen and oxygen gas generated at the end of charging. It's on.
考案が解決しようとする問題点
充電末期に発生するガスを利用した電解液の撹
拌では、ガス発生位置が定つておらず、電解液上
部と下部の硫酸濃度差をなくする程度に十分なも
のではない。実使用時の鉛蓄電池では常に電池の
上部と下部には硫酸濃度差が存在し、上部よりも
下部がより高濃度になる傾向がある。Problems that the invention aims to solve When stirring the electrolyte using the gas generated at the end of charging, the gas generation position is not fixed, and it is not sufficient to eliminate the difference in sulfuric acid concentration between the upper and lower parts of the electrolyte. do not have. In lead-acid batteries in actual use, there is always a difference in sulfuric acid concentration between the top and bottom of the battery, and the concentration tends to be higher in the bottom than in the top.
鉛蓄電池の放電能力は陽極活物質および陰極活
物質のみならず、電解液の硫酸濃度も大きくかか
わつている。一般に同じ性状の活物質を用いた場
合の放電持続時間や放電電圧等の放電特性は、電
解液の硫酸濃度が高ければ高いほど向上する。こ
のことは電池上部と下部で硫酸濃度差のある電解
液中における同一極板にもあてはまり、濃度の高
い極板下部は上部よりも充放電反応が起り易いた
め極板内での不均一が生じ、陽極板では特に下部
の陽極活物質の劣化が優先して起こる。反応の不
均一による局部的な劣化は電池下部や側部での内
部短絡の原因のひとつとなる。 The discharge capacity of a lead-acid battery is greatly affected not only by the anode active material and the cathode active material, but also by the sulfuric acid concentration of the electrolyte. In general, when active materials with the same properties are used, discharge characteristics such as discharge duration and discharge voltage improve as the sulfuric acid concentration of the electrolytic solution increases. This also applies to the same electrode plate in an electrolyte with a difference in sulfuric acid concentration between the upper and lower parts of the battery; charge and discharge reactions occur more easily in the lower part of the plate, where the concentration is higher, than in the upper part, resulting in non-uniformity within the plate. In the case of the anode plate, the deterioration of the anode active material in the lower part takes priority. Local deterioration due to non-uniform reaction is one of the causes of internal short circuits at the bottom and sides of the battery.
一方、硫酸濃度が高い電池において放電で生成
した硫酸鉛は、結晶が大きくなつているため、そ
の充電性が悪い。 On the other hand, lead sulfate produced by discharging in a battery with a high sulfuric acid concentration has large crystals and therefore has poor chargeability.
以上のように、電池内における硫酸濃度の不均
一が鉛蓄電池の性能劣化における重要な因子とな
つてる。 As described above, the non-uniformity of the sulfuric acid concentration within the battery is an important factor in the performance deterioration of lead-acid batteries.
問題点を解決するための手段
本考案は上記問題点を解決するため極板格子体
の下部に水素および酸素発生過電圧の小さな合金
組成よりなるボタン状の部品を取付たものであ
る。Means for Solving the Problems In order to solve the above-mentioned problems, the present invention has a button-shaped component made of an alloy composition with low hydrogen and oxygen generation overvoltage attached to the lower part of the electrode grid.
充電末期の余分な電気量は、抵抗値の小さな導
体(鉛で21×10-6Ωcm、銅を含む鉛合金で20×
10-6Ωcm以下、二酸化鉛で102Ωcm)を電流が流
れ、水分解に費やされるために上記ボタン状に部
品付近から水素および酸素ガスが発生し易くな
る。 The excess electricity at the end of charging is absorbed by conductors with low resistance (21×10 -6 Ωcm for lead, 20× for lead alloys containing copper).
A current of less than 10 -6 Ωcm (10 2 Ωcm for lead dioxide) flows and is used for water decomposition, which tends to generate hydrogen and oxygen gas from near the button-shaped parts.
作 用
本考案は充電末期に発生するガスを主として格
子下部より発生し易くするボタン状の部品を用い
たことにより、電解液の撹拌を促進し、電解液硫
酸濃度を電池上部と下部でより均一にすることが
できる。Function This invention uses a button-shaped part that makes it easier for gas generated at the end of charging to be generated mainly from the bottom of the grid, thereby promoting stirring of the electrolyte and making the concentration of sulfuric acid in the electrolyte more uniform between the top and bottom of the battery. It can be done.
実施例 本考案の一実施例を説明する。Example An embodiment of the present invention will be described.
本考案に用いた格子体1の寸法は高さ130mm、
巾146mm、圧さ3.5mmである。尚格子体下部にとり
つけたボタン状の部品2は円形であり、肉厚は3
mm、その中に4つの穴3があいており中央を電気
溶接によつて格子体1に溶したものである。その
合金組成は格子体1がsb3%残部鉛であるのに対
し、ボタン状部品2はsb5.0%、Cu1.0%残部鉛と
している。 The dimensions of the grid body 1 used in this invention are 130 mm in height.
The width is 146mm and the pressure is 3.5mm. The button-shaped part 2 attached to the lower part of the lattice body is circular, and the wall thickness is 3.
mm, with four holes 3 drilled therein, the center of which is welded to the grid body 1 by electric welding. The alloy composition of the grid body 1 is SB3% balance lead, whereas button-shaped component 2 is SB5.0%, Cu1.0% balance lead.
第2図は鉛蓄電池充電後の高さ方向における電
解液硫酸比重(20℃)の変化を示すものである。
従来品では電流上部と下部との硫酸比重差が大き
く、いわゆる硫酸の成層化現象が著しく観察され
るが、本考案品の格子体下部にボタン状の部品2
を取り付けた格子体1を用いた場合、硫酸比重差
は依然として存在するもののその差は小さくなつ
ている。 Figure 2 shows the change in the electrolyte sulfuric acid specific gravity (20°C) in the height direction after charging the lead-acid battery.
In the conventional product, there is a large difference in the specific gravity of sulfuric acid between the upper and lower parts of the current, and a so-called stratification phenomenon of sulfuric acid is observed, but the product of the present invention has a button-shaped part 2 at the bottom of the grid.
When using the grid body 1 equipped with the sulfuric acid, although the difference in sulfuric acid specific gravity still exists, the difference has become smaller.
第3図は0.6Cの放電電流で1時間放電した後の
陽極活物質中に生成する硫酸鉛(PbSO4)を分析
して求めた結果を示す。従来品では電池上部と下
部に生成するPbSO4量に大きな差が認められる
が、本考案品ではその差は小さい。 FIG. 3 shows the results obtained by analyzing lead sulfate (PbSO 4 ) generated in the anode active material after discharging for one hour at a discharge current of 0.6C. In the conventional product, there is a large difference in the amount of PbSO4 generated at the top and bottom of the battery, but in the product of the present invention, this difference is small.
従来品では充電末期に発生するガスによつて十
分に電解液硫酸の撹拌ができず、著しく成層化し
たまま、次の放電に移るため電池の上部と下部と
では放電によつて生成するPbSO4量に大きな差が
認められる。このため極板内では反応の不均一が
生じていたが、本考案品の場合は、PbSO4量の差
は小さい。 With conventional products, the electrolyte sulfuric acid cannot be sufficiently stirred due to the gas generated at the end of charging, and the electrolyte sulfuric acid remains extremely stratified before proceeding to the next discharge. A large difference in quantity is observed. For this reason, non-uniform reaction occurred within the electrode plate, but in the case of the product of the present invention, the difference in the amount of PbSO 4 was small.
考案の効果
上述したように、格子体下部に取りつけたガス
発生を促進するボタン状の部品を設けることによ
り、充電末期に発生するガスを下部から優先的に
発生させることができる。このため電解液硫酸の
撹拌が従来品よりも十分に行うことができ、電池
の上部と下部の濃度差を小さくすることにより、
極板全体で充放電反応を起こさせることが可能と
なる。即ち反応が特定極板部位にかたよることが
なくなり、極板全体で充放電反応が担われるため
活物質の劣化を抑制し、鉛蓄電池の寿命向上の効
果を有する。 Effects of the Idea As described above, by providing the button-shaped part attached to the lower part of the grid body to promote gas generation, the gas generated at the end of charging can be generated preferentially from the lower part. Therefore, the electrolytic solution sulfuric acid can be stirred more thoroughly than conventional products, and by reducing the concentration difference between the upper and lower parts of the battery,
It becomes possible to cause a charging/discharging reaction in the entire electrode plate. That is, the reaction is no longer concentrated in a specific electrode plate part, and the charge/discharge reaction is carried out by the entire electrode plate, which suppresses deterioration of the active material and has the effect of extending the life of the lead-acid battery.
第1図は本考案の一実施を示す要部斜視図、第
2図は充電後の電解液比重の成層化現象を示す曲
線図、第3図は放電後の極板部位における硫酸鉛
分布を示す曲線図である。
1は格子体、2はボタン状の部品、3は穴。
Figure 1 is a perspective view of the main parts showing one implementation of the present invention, Figure 2 is a curve diagram showing the stratification phenomenon of electrolyte specific gravity after charging, and Figure 3 shows the lead sulfate distribution in the electrode plate area after discharge. FIG. 1 is a grid, 2 is a button-shaped part, and 3 is a hole.
Claims (1)
た陽極板と陰極板の極板群からなる鉛蓄電池にお
いて、前記陽極板または陰極板の格子体の下部に
水素発生過電圧もしくは酸素発生過電圧の小さな
合金よりなるボタン状の部品を取りつけたことを
特徴とする鉛蓄電池。 In a lead-acid battery containing an electrolytic solution of sulfuric acid and consisting of an anode plate and a cathode plate group separated through a separator, an alloy with a small hydrogen generation overvoltage or oxygen generation overvoltage is placed at the bottom of the grid of the anode plate or cathode plate. A lead-acid battery characterized by having a button-shaped part attached.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1986116234U JPH0234757Y2 (en) | 1986-07-29 | 1986-07-29 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1986116234U JPH0234757Y2 (en) | 1986-07-29 | 1986-07-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6323773U JPS6323773U (en) | 1988-02-17 |
JPH0234757Y2 true JPH0234757Y2 (en) | 1990-09-19 |
Family
ID=31000633
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1986116234U Expired JPH0234757Y2 (en) | 1986-07-29 | 1986-07-29 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0234757Y2 (en) |
-
1986
- 1986-07-29 JP JP1986116234U patent/JPH0234757Y2/ja not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS6323773U (en) | 1988-02-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPH06196165A (en) | Sealed lead-acid battery | |
JP4507483B2 (en) | Control valve type lead acid battery | |
JPH0234757Y2 (en) | ||
CN105322238A (en) | Overlapped copper-acid storage battery | |
JPH0234758Y2 (en) | ||
JPH0414758A (en) | Lead-acid accumulator | |
JPS62160659A (en) | Lead storage battery | |
JP2001185151A (en) | Sealed lead acid battery | |
JPH0351890Y2 (en) | ||
JPH05135761A (en) | Lead-acid battery | |
JPH0689738A (en) | Sealed type lead-acid battery | |
JPS58115775A (en) | Lead-acid battery | |
JP2815439B2 (en) | Sealed lead-acid battery | |
JPS59151772A (en) | Manufacture of sealed lead-acid battery | |
JPS6293857A (en) | Manufacture of enclosed lead storage battery | |
JP3614440B6 (en) | High energy battery electrolyte and method for producing the electrolyte | |
JP3614440B2 (en) | High energy battery electrolyte and method for producing the electrolyte | |
JP2021086732A (en) | Positive electrode plate for lead acid battery, and lead acid battery | |
JPH0628782Y2 (en) | Sealed lead acid battery | |
JPS62154579A (en) | Lead-acid battery | |
JP2000058105A (en) | Lead-acid battery | |
JPH0546067B2 (en) | ||
JPH06140042A (en) | Sealed lead-acid battery | |
JP2021086730A (en) | Method for manufacturing positive electrode plate for lead acid battery | |
JPS59138063A (en) | Lead storage battery |