JPH01302656A - Sealed type lead-acid battery - Google Patents
Sealed type lead-acid batteryInfo
- Publication number
- JPH01302656A JPH01302656A JP63132480A JP13248088A JPH01302656A JP H01302656 A JPH01302656 A JP H01302656A JP 63132480 A JP63132480 A JP 63132480A JP 13248088 A JP13248088 A JP 13248088A JP H01302656 A JPH01302656 A JP H01302656A
- Authority
- JP
- Japan
- Prior art keywords
- battery
- separator
- thickness under
- under pressurization
- electrode plate
- 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
Links
- 239000002253 acid Substances 0.000 title claims description 7
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000000463 material Substances 0.000 claims abstract description 8
- 229920002457 flexible plastic Polymers 0.000 claims description 5
- 239000003792 electrolyte Substances 0.000 abstract description 14
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 229920003023 plastic Polymers 0.000 abstract description 2
- 239000004033 plastic Substances 0.000 abstract description 2
- 239000004743 Polypropylene Substances 0.000 abstract 1
- 238000007599 discharging Methods 0.000 abstract 1
- -1 polypropylene Polymers 0.000 abstract 1
- 229920001155 polypropylene Polymers 0.000 abstract 1
- 238000007789 sealing Methods 0.000 abstract 1
- 238000007600 charging Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 238000010280 constant potential charging Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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
- H01M10/34—Gastight accumulators
- H01M10/342—Gastight lead accumulators
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/10—Primary casings; Jackets or wrappings
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M50/00—Constructional details or processes of manufacture of the non-active parts of electrochemical cells other than fuel cells, e.g. hybrid cells
- H01M50/40—Separators; Membranes; Diaphragms; Spacing elements inside cells
- H01M50/489—Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties
-
- 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
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Cell Separators (AREA)
- Sealing Battery Cases Or Jackets (AREA)
Abstract
Description
【発明の詳細な説明】
発明の利用分野
本発明は電槽の少なくとも一面を柔軟性を有するプラス
チック材料により構成した密閉式鉛蓄電池における電池
内圧減少に伴う電槽厚さの変化を極力防止し、電解液の
温液事故を防止するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Application of the Invention The present invention prevents as much as possible changes in the thickness of the battery case due to a decrease in battery internal pressure in a sealed lead-acid battery in which at least one side of the battery case is made of a flexible plastic material. This prevents hot electrolyte accidents.
従来の技術とその問題点
密閉式鉛蓄電池の内圧は放置中に電池内の酸素ガスと負
極板との反応により低下する。また、蓄電池内部には正
極板と負極板を隔離し、電解液を保持するために、一般
に微細繊維セパレータを備えているが、このセパレータ
は容易に圧縮力による変形を生じる。このため、電槽壁
を柔軟性を有するプラスチック材料で構成した密閉式鉛
蓄電池においては、電池内圧の低下に伴い、当該材マ1
が内部方向へ変形し、電解液を保持しているセパレータ
の圧縮変形を生じ、電解液がセパレータより遊離し、排
気孔を通して漏出する危険性がある。Prior art and its problems The internal pressure of a sealed lead-acid battery decreases during storage due to the reaction between the oxygen gas inside the battery and the negative electrode plate. Furthermore, a fine fiber separator is generally provided inside the storage battery in order to isolate the positive electrode plate and the negative electrode plate and to hold the electrolyte, but this separator is easily deformed by compressive force. For this reason, in sealed lead-acid batteries whose container walls are made of flexible plastic materials, as the internal pressure of the battery decreases, the material
is deformed inward, causing compressive deformation of the separator holding the electrolyte, and there is a risk that the electrolyte will be liberated from the separator and leak through the exhaust hole.
このような問題を解決する方法として剛体セパレータの
使用が効果的と考えられるが、電池内のすべての電解液
をセパレータと極板に包含させた構造のリテーナ型密閉
式鉛蓄電池では電池反応を行わせる上で不可欠な■・負
極板と電解液との接触が、実際上、極板とセパレータと
の緊密な接触により実現されるため、剛体セパレータで
は十分な接触を得ることは困難である。The use of rigid separators is thought to be an effective way to solve these problems, but in a cage-type sealed lead-acid battery, which has a structure in which all the electrolyte in the battery is contained in the separator and electrode plates, the battery reaction does not occur. (1) The contact between the negative electrode plate and the electrolyte, which is essential for achieving this, is actually achieved through close contact between the electrode plate and the separator, so it is difficult to achieve sufficient contact with a rigid separator.
また、このような問題の解決法として、予め厚い繊維セ
パレータを用いて電池を作製し、電池が長期間放置され
ても濁液しない量の電解液を注入するという手段が考え
られるが、非常に厚いセパレータを使用する場合には、
組立て時のニレメンI−群長が大きいため、組立て生業
性が悪く、また、電池に注液し、充電した直後では、電
池内圧は低下していないので、セパレータら圧縮されて
いないため、電解液輩はエレメントの保持能力に比べて
著しく少なく、特にセパレータ中の電解液が局部的に分
散して存在するため、極板と電解液との接触が不十分と
なり、満足な放電性能が得られない。In addition, one possible solution to this problem is to fabricate the battery in advance using a thick fiber separator and then inject enough electrolyte so that it will not become cloudy even if the battery is left for a long time, but this is extremely difficult. When using thick separators,
Due to the large Nilemen I-group length during assembly, it is difficult to assemble, and immediately after charging the battery, the internal pressure of the battery has not decreased, so the electrolyte is not compressed by the separator. The electrolyte in the separator is significantly smaller than the holding capacity of the element, and the electrolyte in the separator is locally dispersed, resulting in insufficient contact between the electrode plates and the electrolyte, making it impossible to obtain satisfactory discharge performance. .
問題点を解決するための手段
本発明は電槽の少なくとも一面が柔軟性のあるプラスチ
ック材料により構成された電池において、乾燥状態での
l0Kg/d加圧時の厚さに対して、希硫酸に充分湿潤
した状態での50 K g/dd加圧時の厚さが80%
以上である繊維状セパレータを使用することにより、電
池製作直後から長期放置後に至まで安定した放電性能を
確保すると共に、電池の内圧低下によるセパレータの過
度の圧縮変形に件う漏液の危険性を除去するらのである
。Means for Solving the Problems The present invention provides a battery in which at least one side of the battery case is made of a flexible plastic material, and the thickness of the battery when pressurized with 10 kg/d in a dry state is Thickness is 80% when 50 K g/dd pressure is applied in a sufficiently moist state.
By using the above-mentioned fibrous separator, stable discharge performance is ensured from immediately after battery manufacture to after long-term storage, and the risk of liquid leakage due to excessive compressive deformation of the separator due to a drop in internal pressure of the battery can be ensured. It's time to remove it.
実施例 本発明に関する一実施例について説明する。Example One embodiment of the present invention will be described.
第1図に示す一側面を開放したポリグロビレン製の電槽
1を用い、第2図に示すように側部(開放面)から正極
板2、セパレータ3、負極板4の順に電槽内に積み重ね
た後、柔軟性プラスチック材料5を電槽壁と熱溶着させ
て封目した。尚、セパレータ材料としてはv11細ガラ
ス繊維とプラスチック繊維を混抄したものを用い、従来
品と1.て希硫酸に充分湿潤した状態で50Kg/da
加圧時の厚さと乾燥時の10Kg/dm2加圧時の厚さ
の比が74%(A)のものと77%(B)のものを、ま
た本発明品として上記厚さの比が82%のもの(C)と
86%(D)のらのを用いて電池を製作した。Using a polyglobylene battery case 1 with one side open as shown in Fig. 1, the positive electrode plate 2, separator 3, and negative electrode plate 4 are stacked in the order from the side (open side) inside the case as shown in Fig. 2. After that, the flexible plastic material 5 was thermally welded to the wall of the battery case to seal it. The separator material used is a mixture of V11 fine glass fiber and plastic fiber, and is different from the conventional product and 1. 50Kg/da when fully moistened with dilute sulfuric acid.
The ratio of the thickness when pressurized to the dry thickness when pressurized at 10 kg/dm2 is 74% (A) and 77% (B), and the product of the present invention has a ratio of the above thickness of 82 % (C) and 86% (D) were used to produce batteries.
これらの電池に所定量の希硫酸を注入し、充電した後、
4時間放置および2ケ月放置を憂の0.2C放電性能を
測定した。また、2ケ月放置品については放電後、電池
の排気孔が下方になるように配置し、2.50V /セ
ルで定電圧充電を行い、排気孔からの電解液の漏液の有
無を調べた。これらの結果を表1に示すが、従来品では
初期容iまたは倒置充電での温液のいずれかに問題があ
ったが、本発明品ではいずれも良好な結果が得られた。After injecting a predetermined amount of dilute sulfuric acid into these batteries and charging them,
The 0.2C discharge performance was measured after being left for 4 hours and for 2 months. In addition, for products that had been left for two months, after discharge, the batteries were placed so that the exhaust hole was facing downward, and constant voltage charging was performed at 2.50 V/cell to check for leakage of electrolyte from the exhaust hole. . These results are shown in Table 1. The conventional product had a problem with either the initial volume i or the hot liquid during inverted charging, but the product of the present invention gave good results in both cases.
表 ル
−タ厚さ、t2は乾燥状610Kg/d1!加圧時のセ
パレータ厚さである。Table Thickness of router, t2 is 610Kg/d1 in dry state! This is the separator thickness when pressurized.
注2.初期容量は充電4時間後の容量、放置後容量は2
ケ月放置後の容量である。Note 2. The initial capacity is the capacity after 4 hours of charging, and the capacity after being left is 2.
This is the capacity after being left unused for several months.
発明の効果
以上述べたように、本発明による密閉式鉛M電池では常
に安定な放電容量を有し、かつ電解液の漏洩の危険性を
除去でき、その工業的価値は大きい。Effects of the Invention As described above, the sealed lead-acid M battery according to the present invention always has a stable discharge capacity and can eliminate the risk of electrolyte leakage, and has great industrial value.
第1図は試験に用いた一側面を開口I7た電槽の構造を
示ず図、第2図は試@電池の要部4JI断面図である。
1・・・・・・電#!J 2・・・・・・正極
板3・・・・・・セパレータ 4・・・・・・負極板
5・・・・・・熱溶着により電槽側壁を封目した柔軟性
に″゛2.ン
輝 Z 回FIG. 1 is a diagram not showing the structure of a battery case with an opening I7 on one side used in the test, and FIG. 2 is a cross-sectional view of the main part 4JI of the test battery. 1... Telephone number! J 2...Positive electrode plate 3...Separator 4...Negative electrode plate 5...Flexibility that seals the side wall of the battery case by heat welding ``゛2 .Nuki Z times
Claims (1)
により構成された電池において、乾燥状態での10Kg
/dm^2加圧時の厚さに対して希硫酸に充分湿潤した
状態での50Kg/dm^2加圧時の厚さが80%以上
である繊維状セパレータを使用することを特徴とする密
閉式鉛蓄電池。In a battery where at least one side of the battery case is made of flexible plastic material, the weight in dry state is 10Kg.
It is characterized by using a fibrous separator whose thickness when pressurized at 50 kg/dm^2 is 80% or more of the thickness when pressurized with dilute sulfuric acid. Sealed lead acid battery.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63132480A JPH01302656A (en) | 1988-05-30 | 1988-05-30 | Sealed type lead-acid battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP63132480A JPH01302656A (en) | 1988-05-30 | 1988-05-30 | Sealed type lead-acid battery |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01302656A true JPH01302656A (en) | 1989-12-06 |
Family
ID=15082360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP63132480A Pending JPH01302656A (en) | 1988-05-30 | 1988-05-30 | Sealed type lead-acid battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01302656A (en) |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51101837A (en) * | 1975-03-05 | 1976-09-08 | Yuasa Battery Co Ltd | |
JPS5553064A (en) * | 1978-10-13 | 1980-04-18 | Japan Storage Battery Co Ltd | Closed-type lead accumulator |
-
1988
- 1988-05-30 JP JP63132480A patent/JPH01302656A/en active Pending
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51101837A (en) * | 1975-03-05 | 1976-09-08 | Yuasa Battery Co Ltd | |
JPS5553064A (en) * | 1978-10-13 | 1980-04-18 | Japan Storage Battery Co Ltd | Closed-type lead accumulator |
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