JPS62208568A - Paste type lead-acid battery - Google Patents

Paste type lead-acid battery

Info

Publication number
JPS62208568A
JPS62208568A JP61051258A JP5125886A JPS62208568A JP S62208568 A JPS62208568 A JP S62208568A JP 61051258 A JP61051258 A JP 61051258A JP 5125886 A JP5125886 A JP 5125886A JP S62208568 A JPS62208568 A JP S62208568A
Authority
JP
Japan
Prior art keywords
lead
electrolyte
acid battery
type lead
paste type
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.)
Pending
Application number
JP61051258A
Other languages
Japanese (ja)
Inventor
Akio Tokunaga
徳永 昭夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Japan Storage Battery Co Ltd
Original Assignee
Japan Storage Battery Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Japan Storage Battery Co Ltd filed Critical Japan Storage Battery Co Ltd
Priority to JP61051258A priority Critical patent/JPS62208568A/en
Publication of JPS62208568A publication Critical patent/JPS62208568A/en
Pending legal-status Critical Current

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M10/00Secondary cells; Manufacture thereof
    • H01M10/06Lead-acid accumulators
    • H01M10/08Selection of materials as electrolytes
    • 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

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

PURPOSE:To prevent early capacity drop in deep charge-discharge cycles by adding a potassium salt of higher fatty acid to an electrolyte. CONSTITUTION:In a paste type lead-acid battery using a lead-calcium group alloy grid, a potassium salt of higher fatty acid is added to an electrolyte. By adding this salt to the electrolyte, early capacity drop in deep charge- discharge cycles which is a problem in a paste type lead-acid battery using lead-calcium group alloy grid can be prevented.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は鉛−カルシウム系合金格子を用いたペースト式
鉛蓄電池に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a paste type lead-acid battery using a lead-calcium alloy lattice.

従来の技術 鉛蓄電池に用いられるペースト式極板の格子は、これま
で鉛−アンチモン系合金が使われてきたが、電池の無保
守化に対する要求から鉛−カルシウム系合金が多用され
るようになってきた。鉛−カルシウム系合金を格子に使
うと、電池の自己放電が少なく、電解液の減少が少ない
ので、補水の必要がなくなる等の長所を右する反面、深
い充放電を繰返すと、従来の鉛−アンチモン系合金では
みられなかった電池容量が早期に低下するという重大な
欠点が生じた。これは、電池の充放電によって格子と工
種活物質との間に電気の不良導体が形成されることに起
因すると言われている。この欠点を解消するために種々
の12案がなされているが、いまだに問題の解消には至
っていない。
Conventional technology Lead-antimony based alloys have been used for the grids of paste-type electrode plates used in lead-acid batteries, but lead-calcium based alloys are increasingly being used due to the demand for maintenance-free batteries. It's here. Using a lead-calcium alloy for the grid has advantages such as less self-discharge of the battery and less loss of electrolyte, eliminating the need for water replenishment. A serious drawback, which was not observed with antimony-based alloys, was an early decline in battery capacity. This is said to be caused by the formation of a poor electrical conductor between the grid and the active material during charging and discharging of the battery. Twelve various proposals have been made to solve this drawback, but the problem has not yet been solved.

問題点を解決するための手段 本発明は鉛−カルシウム系合金格子を用いたペースト式
鉛蓄電池の電解液に高級脂肪酸のカリウム塩を添加する
ことにより、上記従来の欠点を解消し、深い充放電を繰
返しても早期容量低下の起りにくいペースト式鉛蓄電池
を提供しようとするものである。
Means for Solving the Problems The present invention solves the above-mentioned conventional drawbacks by adding a potassium salt of higher fatty acids to the electrolyte solution of a paste type lead-acid battery using a lead-calcium alloy lattice, and enables deep charging and discharging. The purpose of the present invention is to provide a paste-type lead-acid battery that is unlikely to experience early capacity loss even after repeated use.

実施例 以下に本発明の詳細な説明する。Example The present invention will be explained in detail below.

本実施例では高級脂肪酸のカリウム塩として力り石鹸を
用いた。まず、所定圀のカリ石鹸を精製水に溶かし、つ
いでVIiI!酸を加えて比重1.20の電解液を調製
した。この電解液を工種および負極とも鉛−カルシウム
合金からなる公称容11sAh(5hR)自動車用船N
TX池に注液し、正極活物質の理論容量に対して300
%の電気間で初充電を行なった。比較のために、高級脂
肪酸のカリウム塩を添加しない電解液を注液して、同様
の条件で初充電を行った従来品も次の試験に供した。試
験は充?!後の電解液比重を1.28に調整したのち、
5hR電流(5,6へ)で1.75V/セルまで放電し
、放電後の充電は放電容量の130%を10時間で充電
するというパターンの充放電繰り返しで、その試験結果
を第1図に示す。図において、Aは電解液に高級脂肪酸
のカリウム塩を添加しない従来品、BとCはそれぞれ電
解液に高級脂肪酸のカリウム塩としてカリ石鹸を電解液
に対して0.1Q/Qおよび0.5 り/l (K″′
として57 mg/免および284 mQ/λ)添加し
た本発明品である。従来品はサイクルとともに容量が低
下し、10サイクル後には初期の50%以下の容量とな
った。一方、本発明品BおよびCは充放電サイクルによ
る容届低下は少なく、カルシウム電池特有の早期容量低
下はみられなかった。
In this example, strength soap was used as the potassium salt of higher fatty acid. First, dissolve the potash soap from the specified area in purified water, then VIiI! An electrolytic solution having a specific gravity of 1.20 was prepared by adding an acid. This electrolyte was used for a car carrier with a nominal capacity of 11 sAh (5 hR), which was made of a lead-calcium alloy for both the construction type and the negative electrode.
Pour the liquid into the TX pond and add 300% to the theoretical capacity of the positive electrode active material.
The first charge was performed with % electricity. For comparison, a conventional product was also subjected to the next test, in which an electrolytic solution without the addition of potassium salts of higher fatty acids was injected and initial charging was performed under similar conditions. Is the exam complete? ! After adjusting the electrolyte specific gravity to 1.28,
The test results are shown in Figure 1 by repeating the charging and discharging pattern of discharging to 1.75V/cell with a 5hR current (to 5 and 6), and charging after discharging to 130% of the discharge capacity in 10 hours. show. In the figure, A is a conventional product in which no potassium salt of a higher fatty acid is added to the electrolyte, B and C are a conventional product in which a potassium salt of a higher fatty acid is added to the electrolyte, and potassium soap is added to the electrolyte at 0.1Q/Q and 0.5, respectively. ri/l (K″′
This is the product of the present invention in which 57 mg/immune and 284 mQ/λ) were added. The capacity of the conventional product decreased with each cycle, and after 10 cycles, the capacity was less than 50% of the initial capacity. On the other hand, products B and C of the present invention showed little decrease in performance due to charge/discharge cycles, and no early capacity decrease peculiar to calcium batteries was observed.

なお、実施例では高級脂肪酸のカリウム塩をに1としテ
57rngl交および248 m1ll/ l添加した
場合の実施例を示したが、30 m(1/λ〜1000
 mgZ見の範囲で効果があった。
In addition, in the example, an example was shown in which potassium salt of higher fatty acid was added to 1, 57 rngl and 248 ml/l, but 30 m (1/λ~1000
It was effective within the range of mgZ.

発明の効果 実施例で明らかなように、本発明によれば電解液に高級
脂肪酸のカリウム塩を添加するだけで、鉛カルシウム系
合金格子を用いたペースト式鉛蓄電池の欠点であった深
い充放電サイクルでの早期容量低下を防止でき、その工
業的価値は大きい。
Effects of the Invention As is clear from the examples, according to the present invention, by simply adding potassium salts of higher fatty acids to the electrolyte, deep charging and discharging, which was a drawback of paste-type lead-acid batteries using lead-calcium alloy grids, can be achieved. It can prevent early capacity reduction during the cycle, and its industrial value is great.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明品と従来品の充放電サイクル性能を比較
したものである。
FIG. 1 compares the charge/discharge cycle performance of the product of the present invention and the conventional product.

Claims (1)

【特許請求の範囲】[Claims] 1、電解液に高級脂肪酸のカリウム塩を添加することを
特徴とする鉛−カルシウム系合金格子を用いたペースト
式鉛蓄電池。
1. A paste-type lead-acid battery using a lead-calcium alloy lattice characterized by adding a potassium salt of a higher fatty acid to the electrolyte.
JP61051258A 1986-03-07 1986-03-07 Paste type lead-acid battery Pending JPS62208568A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61051258A JPS62208568A (en) 1986-03-07 1986-03-07 Paste type lead-acid battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61051258A JPS62208568A (en) 1986-03-07 1986-03-07 Paste type lead-acid battery

Publications (1)

Publication Number Publication Date
JPS62208568A true JPS62208568A (en) 1987-09-12

Family

ID=12881919

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61051258A Pending JPS62208568A (en) 1986-03-07 1986-03-07 Paste type lead-acid battery

Country Status (1)

Country Link
JP (1) JPS62208568A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2280443A1 (en) * 2008-05-20 2011-02-02 GS Yuasa International Ltd. Lead storage battery and process for producing the lead storage battery
CN103700847A (en) * 2013-11-30 2014-04-02 安徽轰达电源有限公司 Formula of polar plate lead plaster with high energy storage capacity, long service life and low temperature resistance

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2280443A1 (en) * 2008-05-20 2011-02-02 GS Yuasa International Ltd. Lead storage battery and process for producing the lead storage battery
EP2280443A4 (en) * 2008-05-20 2012-04-04 Gs Yuasa Int Ltd Lead storage battery and process for producing the lead storage battery
CN103700847A (en) * 2013-11-30 2014-04-02 安徽轰达电源有限公司 Formula of polar plate lead plaster with high energy storage capacity, long service life and low temperature resistance

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