JPS5951485A - Charging process of enclosed lead storage battery - Google Patents
Charging process of enclosed lead storage batteryInfo
- Publication number
- JPS5951485A JPS5951485A JP57162490A JP16249082A JPS5951485A JP S5951485 A JPS5951485 A JP S5951485A JP 57162490 A JP57162490 A JP 57162490A JP 16249082 A JP16249082 A JP 16249082A JP S5951485 A JPS5951485 A JP S5951485A
- Authority
- JP
- Japan
- Prior art keywords
- oxygen
- charging
- oxygen gas
- concentration
- current
- 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.)
- Granted
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
- H01M10/42—Methods or arrangements for servicing or maintenance of secondary cells or secondary half-cells
- H01M10/44—Methods for charging or discharging
-
- 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
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Secondary Cells (AREA)
Abstract
Description
【発明の詳細な説明】
本発明はアンチモンを含まない鉛合金格子を用い1こ密
閉形鉛蓄電池の充電方法に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for charging a single sealed lead acid battery using an antimony-free lead alloy grid.
酸素サイクル反応による密閉形鉛蓄電池には電解液の水
の損失を防ぐ1こめに、通常鉛−カルシウムなどのアン
チモンを含まない鉛合金が格子に用いられている。この
種の合金を用いた正−仮は、−酸化鉛などの電気絶縁性
物質が格子と活物質との界面に生成する、いわゆるバリ
ヤーによって早期に寿命に至ることがある。Sealed lead-acid batteries based on oxygen cycling reactions typically use antimony-free lead alloys, such as lead-calcium, in the grid to prevent loss of electrolyte water. A positive electrode using this type of alloy may reach the end of its life prematurely due to the formation of a so-called barrier, in which an electrically insulating material such as -lead oxide forms at the interface between the lattice and the active material.
本発明はこのバリヤー生成の原因を研究し、新規な光電
方法によってその生成を防いだもので、密閉形鉛蓄電池
を安定して長寿命化することを目的としている。The present invention investigates the cause of this barrier formation and prevents its formation using a novel photoelectric method, and aims to stably extend the life of sealed lead-acid batteries.
本発明の要旨は、セル円空間の酸素濃度を検出し、その
値が極大を経てのち所定値以下となつTことき充電電流
を切ることにある。The gist of the present invention is to detect the oxygen concentration in the cell circular space, and to cut off the charging current when the oxygen concentration reaches a maximum and then falls below a predetermined value.
酸素サイクル反応による電池では、セル円空間の気相が
負−活物質と接曽オる構成である。この気相中の酸素ガ
スの濃度を種々変えて放置しTこときの正To板の劣化
状態を調べて@1表に示す。In a battery based on an oxygen cycle reaction, the gas phase in the cell circular space is in contact with the negative active material. The deterioration state of the T-shaped To plate was examined by changing the concentration of oxygen gas in the gas phase and leaving it for a while, and the results are shown in Table 1.
放置条件は温度50℃で1ケ月であり、正−板の性能は
10分間率放電容量によって表しrこ。The storage conditions were 1 month at a temperature of 50°C, and the performance of the main plate was expressed by the 10 minute rate discharge capacity.
@1表
表から明らかなようiこ酸素ガスの分圧が0.08気田
以下ではまつTコ<劣化が認められないが、02気田以
上では著しく劣化している。この理由はセル内空間の酸
素ガスが格子表面を酸化してバリヤーを形成させrこと
考えらnる。しTこがってこの劣化を防ぐには、電池の
放電中のセル内空間の酸素ガス分圧が01気圧以下にな
るようにすればよい。As is clear from Table 1, no deterioration is observed when the partial pressure of oxygen gas is 0.08 or less, but it is significantly degraded when it is 0.2 or more. The reason for this is thought to be that oxygen gas in the space within the cell oxidizes the lattice surface to form a barrier. However, in order to prevent this deterioration, the partial pressure of oxygen gas in the space within the cell during discharge of the battery may be set to 0.1 atm or less.
つぎにセル内空間の酸素ガスの分圧と、10 時間率放
電電流の−の微小電流で充電しγこときの正陽板の劣化
軟融を調べた結果を第2表に示す。Next, Table 2 shows the results of investigating the partial pressure of oxygen gas in the cell interior space and the deterioration and softening of the positive plate of the γ cell by charging with a minuscule current of 10 hour rate discharge current.
充電条件は温度80℃の雰囲気中で1ケ月行ない、正I
!ll仮の性能はlO分間率放電容量によって表し1こ
。The charging conditions were one month in an atmosphere with a temperature of 80°C, and a positive I
! The tentative performance is expressed by the minute rate discharge capacity.
第2表
表から明らかなように、正−仮は酸素ガスの分圧の値の
大小によらず、はとんど劣化していない。As is clear from Table 2, there is almost no deterioration in the positive and temporary cases, regardless of the magnitude of the partial pressure of oxygen gas.
さらに、10 時間率放電電流の4 の電流で充電し1
ごときのセル内空間の酸素ガスの分圧変化を調べTこ結
果を第1図に示す。この充電の前には10時間率で完全
放電し1こ。酸素ガスの分子は化電電気量の約90 %
のときに砥大を示し、μ後は充電の進行につれて低下し
てゆく。Furthermore, charge at a current of 4 times the discharge current at a rate of 10 hours.
The changes in the partial pressure of oxygen gas in the cell interior space were investigated and the results are shown in FIG. Before this charge, completely discharge the battery at a rate of 10 hours. Oxygen gas molecules account for approximately 90% of the electrical charge
The abrasive strength is indicated when , and after μ it decreases as charging progresses.
以上の結果から、光電電流を適当に選べば、セル内空間
の酸素ガスの分圧をかなり低く抑えることが可能であり
、酸素ガスの分圧を低く抑え1このち充電電流を切れば
、モ陽仮の劣化は噸くなる。From the above results, if the photoelectric current is selected appropriately, it is possible to keep the partial pressure of oxygen gas in the space inside the cell quite low. The deterioration of Yangkari becomes ridiculous.
つぎに本発明を第2図に示す一実施例によって説明する
。(1)は電槽および蓋、(2)は正1仮、(8)は負
陽板、(4)はセパレータ、(5)は保液体で、珪酸ゲ
ルやガラスIa帷からなるマットなどより構成され希硫
酸を保持している。(6)は酸素ガスの分圧を測定する
セッサー、(7)は排気部、181は酸素ガスの分圧に
応じて電流や!田を制御する機能を持つ1こ充電器であ
る。Next, the present invention will be explained with reference to an embodiment shown in FIG. (1) is the battery case and lid, (2) is the positive 1 temporary, (8) is the negative positive plate, (4) is the separator, and (5) is the liquid retaining material. It contains dilute sulfuric acid. (6) is a sensor that measures the partial pressure of oxygen gas, (7) is an exhaust section, and 181 is a current that changes depending on the partial pressure of oxygen gas. This is a single charger that has the function of controlling the rice field.
第8辰は1ケ月ごとに2回答蝋試験を行なうという断続
的なサイクル試験結果を示す。光電方法ハtA11.t
10 hR定tmテ放″II1.Wt電気量120%
、(B)はjft 大!fiハ10 hR、最大Wl
rfハ2.40 V/ セルCD定電流・疋電子で16
時間、(C)は本発明になるもので、10htt疋Wl
流で光Ill、セル内の酸素ガス分圧が崗大をすぎfこ
ところで2.40 V /セルの疋電圧光wLIζ切換
え、さらに酸素ガス分圧が0.08気げに低下しfこと
きに充電を終了する方法とし1こ。Section 8 shows the results of an intermittent cycle test in which a two-response wax test is conducted every month. Photoelectric method HatA11. t
10 hR constant tm discharge'' II 1.Wt electricity amount 120%
, (B) is jft large! fiha 10 hR, maximum Wl
RF: 2.40 V/cell CD constant current/electronic: 16
Time, (C) is according to the present invention, 10httWl
With the current, the partial pressure of the oxygen gas in the cell exceeds 2.40 V/cell, and the voltage of the light changes to 2.40 V/cell, and the partial pressure of the oxygen gas decreases to about 0.08. Here's how to end charging.
第 3 表
5一
本発明による方法で充電し1こものは86 ケバ後もほ
とんど容量の低下はないが、単なる定電流あるいは定電
流・疋電王光電のものは約80 ケ月以降かなりの容量
低下があるう
以上のように本発明は密閉形鉛蓄電池の正―板の劣化を
充電方法によって改善しfこものである。Table 3: Charged by the method according to the present invention, there is almost no decrease in capacity even after 86 months, but for simple constant current or constant current Hikideno Koden batteries, the capacity decreases considerably after about 80 months. As described above, the present invention improves the deterioration of the positive plate of a sealed lead-acid battery by using a charging method.
第1閏は児電電気竜とセル内空間の酸素ガス分子との関
係を示す特性図、ij!2図は本発明になる鉛蓄電池を
示す要部縦断面図模式図である。
2・・・・・・正慟板、 8・・・・・・負働板、 4
・・・・・・セパレータ、 5・・・・・・保液体、
6・・・・・・酸素ガスの分圧測定センサー、 8・
・・・・・充電器。
6一
斉 1 目
get九量(%)
A Z 図The first leap is a characteristic diagram showing the relationship between Koden Denryu and oxygen gas molecules in the space inside the cell, ij! FIG. 2 is a schematic longitudinal cross-sectional view of the main parts of the lead-acid battery according to the present invention. 2...Positive plate, 8...Negative plate, 4
... Separator, 5 ... Liquid retention,
6... Oxygen gas partial pressure measurement sensor, 8.
...Charger. 6 all at once 1st get 9 amount (%) A Z diagram
Claims (1)
経てのち所定値以下となつTことき電流を切る密閉形鉛
蓄電池の光電方法。 (2) 酸素濃度が所定の値以上となるかまTコは1
大を経Tコときに電流を減衰させる特許請求の範囲第(
1)項記載の密閉形鉛蓄電池の充電方法。[Claims] (Photoelectric method for a sealed lead-acid battery that detects the oxygen concentration in a circular space of 11 cells and cuts off the current when the value reaches a small value and then drops below a predetermined value. (2) Oxygen concentration is greater than a predetermined value, the hook T is 1
Claim No. 2 (
1) Method for charging a sealed lead-acid battery as described in section 1).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57162490A JPS5951485A (en) | 1982-09-18 | 1982-09-18 | Charging process of enclosed lead storage battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57162490A JPS5951485A (en) | 1982-09-18 | 1982-09-18 | Charging process of enclosed lead storage battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5951485A true JPS5951485A (en) | 1984-03-24 |
JPH0352189B2 JPH0352189B2 (en) | 1991-08-09 |
Family
ID=15755602
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57162490A Granted JPS5951485A (en) | 1982-09-18 | 1982-09-18 | Charging process of enclosed lead storage battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5951485A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS622905A (en) * | 1985-06-29 | 1987-01-08 | 株式会社 サンギ | Toothbrush |
US5441536A (en) * | 1991-06-18 | 1995-08-15 | Kabushiki Kaisya Advance | Method for the production of an implant having an apatite coating layer using a hydrothermal treatment |
-
1982
- 1982-09-18 JP JP57162490A patent/JPS5951485A/en active Granted
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS622905A (en) * | 1985-06-29 | 1987-01-08 | 株式会社 サンギ | Toothbrush |
US5441536A (en) * | 1991-06-18 | 1995-08-15 | Kabushiki Kaisya Advance | Method for the production of an implant having an apatite coating layer using a hydrothermal treatment |
Also Published As
Publication number | Publication date |
---|---|
JPH0352189B2 (en) | 1991-08-09 |
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