JPH0624143B2 - Sealed lead acid battery - Google Patents
Sealed lead acid batteryInfo
- Publication number
- JPH0624143B2 JPH0624143B2 JP63211524A JP21152488A JPH0624143B2 JP H0624143 B2 JPH0624143 B2 JP H0624143B2 JP 63211524 A JP63211524 A JP 63211524A JP 21152488 A JP21152488 A JP 21152488A JP H0624143 B2 JPH0624143 B2 JP H0624143B2
- Authority
- JP
- Japan
- Prior art keywords
- active material
- electrolytic solution
- acid battery
- sealed lead
- negative electrode
- 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 - Lifetime
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
- H01M10/06—Lead-acid accumulators
- H01M10/12—Construction or manufacture
- H01M10/126—Small-sized flat cells or batteries for portable equipment
-
- 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
- H01M50/116—Primary casings; Jackets or wrappings characterised by the material
- H01M50/121—Organic material
-
- 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
-
- 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
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)
- Battery Electrode And Active Subsutance (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は薄形の密閉形鉛蓄電池に関するものである。TECHNICAL FIELD The present invention relates to a thin sealed lead acid battery.
従来の技術 従来の密閉形鉛蓄電池は、鉛格子、鉛シートの全面に活
物質を充填した正、負極板を電解液保持体をはさんで積
層する構造である。2. Description of the Related Art A conventional sealed lead-acid battery has a structure in which positive and negative electrode plates in which the entire surface of a lead grid and a lead sheet are filled with an active material are sandwiched with an electrolyte solution holder.
発明が解決しようとする課題 一般に、鉛蓄電池はPhO2+Pb+2H2SO4 2PbSO4 +2
H2O の反応で進行する。すなわち活物質としてはPbO2、
Pbだけでなく、電解液のH2SO4 も活物質となる。ところ
でその3種の密度はポーラスなPbO2で約3〜4g/c
m3、ポーラスPbで3〜4g/cm3、aq2H2SO4 で1.2
〜1.3g/cm3である。すなわち電極のPbO2、Pbの密
度にくらべ電解液の密度が小さい。また1Ahに必要な重
量はPbO2で 4.463g、Pbで3.87g、比重1.3aqH2SO4
で9.33gであるゆえ、1Ahに必要な電池としての活物質
体積はPbO2で1.12〜1.48cm3、Pbで0.97〜1.29cm3、比重
1.3のaqH2SO4 で7.18cm3となる。これから解るよう
に電解液の占有体積が電極体積にくらべ非常に大きい。
ところで鉛蓄電池の場合、必要な電解液占有空間を確保
しても電解液が活物質であるためその拡散に限度があ
り、有効に活用されない。すなわち電解液の拡散が支配
因子となり、そのため、従来の密閉形鉛蓄電池ではその
活物質利用率としてPbO2で25〜35%、Pbで27〜40%、電
解液で80〜95%と電極の活物質の利用率が低い設計とな
っている。そのために他の電池に比べエネルギー密度が
向上できないでいる。そこで支配的である電解液の拡散
を高め電極の活物質中へのH2SO4の供給を高め、エネル
ギー密度を向上させる必要がある。従来の密閉形鉛蓄電
池ではPbO2活物質層、電解液保持層、Pb活物質層が積層
される形となっており、電池放電中のH2SO4 の拡散、供
給は常に一方向の動きに制限されるため、拡散が追いつ
かずPbO2、Pb活物質の内部まで放電反応が進むことなく
表面層のみ反応に関与することとなる。Problems to be Solved by the Invention In general, lead-acid batteries have PhO 2 + Pb + 2H 2 SO 4 2PbSO 4 +2
The reaction proceeds with H 2 O. That is, PbO 2 as the active material,
Not only Pb but also H 2 SO 4 in the electrolytic solution becomes the active material. Meanwhile density of the three is approximately in porous PbO 2 3 to 4 g / c
m 3, a porous Pb in 3~4g / cm 3, aq2H 2 SO 4 1.2
~ 1.3 g / cm 3 . That is, the density of the electrolytic solution is lower than the density of PbO 2 and Pb of the electrode. The weight required for 1 Ah is 4.463 g for PbO 2 , 3.87 g for Pb, and the specific gravity is 1.3aqH 2 SO 4
In because it is 9.33g, 1.12~1.48cm the active material volume PbO 2 as a battery required 1Ah 3, 0.97~1.29cm in Pb 3, the 7.18Cm 3 in aqH 2 SO 4 of specific gravity 1.3 . As can be seen, the occupied volume of the electrolytic solution is much larger than the electrode volume.
By the way, in the case of a lead storage battery, even if a required electrolyte solution occupying space is secured, the electrolyte solution is an active material, so its diffusion is limited and cannot be effectively utilized. That is, the diffusion of the electrolytic solution becomes the controlling factor, and therefore, in the conventional sealed lead-acid battery, the active material utilization rate is 25 to 35% for PbO 2 , 27 to 40% for Pb, and 80 to 95% for the electrolytic solution. It is designed to have a low utilization rate of active material. Therefore, the energy density cannot be improved as compared with other batteries. Therefore, it is necessary to enhance the diffusion of the electrolytic solution, which is dominant, to enhance the supply of H 2 SO 4 into the active material of the electrode, and to improve the energy density. In the conventional sealed lead-acid battery, the PbO 2 active material layer, the electrolyte holding layer, and the Pb active material layer are laminated, and the diffusion and supply of H 2 SO 4 during battery discharge always moves in one direction. Therefore, only the surface layer is involved in the reaction without the diffusion reaction catching up and the discharge reaction not proceeding to the inside of the PbO 2 and Pb active materials.
課題を解決するための手段 本発明は、正極集電体上に正極活物質を、負極集電体上
に負極活物質をそれぞれ多数の角形状または丸形状を成
形させ、各極活物質間に電解液保持体を配した正、負極
板が電解液保持体を介して積層され、電解液と共に密閉
されたことを特徴とするものである。Means for Solving the Problems The present invention is to form a positive electrode active material on a positive electrode current collector and a negative electrode active material on a negative electrode current collector into a large number of angular shapes or circular shapes, respectively, and It is characterized in that the positive and negative electrode plates on which the electrolytic solution holders are arranged are laminated via the electrolytic solution holders and sealed together with the electrolytic solution.
作用 本発明は上記の特徴を有することにより、電解液の拡
散、供給が従来の密閉形鉛蓄電池の一方向の動きでな
く、上下、左右の方向の動きが得られるため、電極活物
質の反応が表面層にとどまらず内部まで可能となり、利
用率が大幅に向上し、エネルギー密度の向上が図れる。Action The present invention has the above-described characteristics, so that the diffusion and supply of the electrolytic solution do not move in one direction in the conventional sealed lead-acid battery but move in the vertical and horizontal directions. Can be applied not only to the surface layer but also to the inside, greatly improving the utilization rate and improving the energy density.
実施例 本発明の一実施例を説明する。Example An example of the present invention will be described.
第1図、第2図に示す如く、樹脂フィルム1上に鉛ミー
トからなる正極集電体2を接着し、その上にスクリーン
印刷によって正極活物質4を正方形状に配し、その後こ
の正極活物質4間に、電解液保持体3としてシリ化ゲル
状電解液を同じくスクリーン印刷により塗着して正極板
が得られる。同様にして得られた負極板との間にさらに
電解液保持体3としてのガラス繊維不織布をはさみ、積
層して樹脂フィム1,1′の周囲を熱溶着して溶着部6
を形成し、電解液と共に封した。ここでは各活物質間の
同一平面に塗着した電解液保持体3としてシリカゲル状
電解液を用いたが、もちろんここもガラス繊維不織布と
しても良い。本発明品として、厚さ3mmの密閉形鉛蓄電
池を作成し、従来の集電体の全面に活物質を充填した
正、負極板を電解液保持体をはさんで積層してフィルム
パックの密閉形鉛蓄電池を 100%としたときの活物質利
用率の比較を行った。放電は0.1C相当、2C相当の
電熱で行い、電解液比重は 1.350を使用した。第3図、
第4図にそれぞれの結果を示す。図から明らかなように
本発明品は、利用率として0.1C放電の場合、PbO2で
約25%、Pbで約20%H2SO4 で約5%上昇している。特に
2C放電のような高率放電の場合は、それぞれそ約35
%、30%、10%となり、その利用率向上率は著しい。さ
らに電極活物質が均一的に利用されるため、従来の極板
のように表面層に反応が集中せず、長寿命化が期待され
る。As shown in FIGS. 1 and 2, a positive electrode current collector 2 made of lead meat is bonded onto a resin film 1, and a positive electrode active material 4 is arranged in a square shape by screen printing on the positive electrode current collector 2. A silylated gel electrolyte solution is similarly applied by screen printing as an electrolyte solution holder 3 between the substances 4 to obtain a positive electrode plate. A glass fiber non-woven fabric as the electrolytic solution holder 3 was further sandwiched between the negative electrode plate and the negative electrode plate obtained in the same manner, and the layers were laminated and heat-welded around the resin film 1, 1 ′ to form a welded portion 6
Was formed and sealed with the electrolyte. Here, a silica gel-like electrolytic solution is used as the electrolytic solution holder 3 applied on the same plane between the active materials, but of course, a glass fiber non-woven fabric may also be used here. As a product of the present invention, a sealed lead-acid battery having a thickness of 3 mm was prepared, and a positive electrode plate and a negative electrode plate, which were filled with an active material on the entire surface of a conventional current collector, were laminated with an electrolytic solution holder between them to seal a film pack. The active material utilization rate was compared when the lead acid battery was set to 100%. The discharge was performed by electric heat equivalent to 0.1 C and 2 C, and the specific gravity of the electrolyte was 1.350. Figure 3,
Each result is shown in FIG. As is apparent from the figure, in the case of 0.1 C discharge, the utilization rate of the product of the present invention increased by about 25% for PbO 2 , about 20% for Pb, and about 5% for H 2 SO 4 . Especially in case of high rate discharge such as 2C discharge, it is about 35
%, 30%, 10%, and the rate of improvement in utilization rate is remarkable. Furthermore, since the electrode active material is uniformly used, the reaction is not concentrated on the surface layer unlike the conventional electrode plate, and it is expected that the life is extended.
なお、本実施例は正方形状に活物質を形成させたが、三
角形、六角形状、他の多角形状、または円形、楕円形状
他の丸形状でも同様な効果が得られる。Although the active material is formed in a square shape in the present embodiment, the same effect can be obtained by using a triangular shape, a hexagonal shape, another polygonal shape, or a circular shape, an elliptical shape, or another circular shape.
発明の効果 上述のように、本発明の密閉形鉛蓄電池は従来の電池と
は異なり、電極活物質を分割しその間に電解液保持体を
有し、さらに対極との間にも電解液保持体を有するた
め、電解液の拡散供給が上下、左右方向から得られ、電
極活物質の内部まで反応が進み電極活物質の利用率を向
上させることができる。その為、電極活物質量を減ずる
ことが可能で、特に重量エネルギー密度向上に極めて有
効である。また長寿命化も期待される。Effect of the Invention As described above, the sealed lead-acid battery of the present invention is different from the conventional battery in that the electrode active material is divided and the electrolytic solution holding body is provided between them, and the electrolytic solution holding body is also provided between the electrode and the counter electrode. Therefore, the diffusion and supply of the electrolytic solution can be obtained in the vertical and horizontal directions, the reaction can proceed to the inside of the electrode active material, and the utilization rate of the electrode active material can be improved. Therefore, it is possible to reduce the amount of the electrode active material, and it is extremely effective for improving the weight energy density. It is also expected to have a long life.
さらに、スクリーン印刷技術と適用が可能であり、作成
面でも自動化、省力化が可能となり、容易に薄形の密閉
形鉛蓄電池を製造できる等工業的価値極めて大なるもの
である。Furthermore, it can be applied to screen printing technology, can be automated and labor-saving in terms of production, and can be easily manufactured into a thin sealed lead-acid battery, which is of great industrial value.
第1図は本発明の一実施例を示す密閉形鉛蓄電池の断面
図、第2図は本発明の一実施例における正極板を示す平
面図、第3図は0.1C放電時の活物質利用率比較図、
第4図は2C放電時の活物質利用率比較図である。 1、1′は樹脂フィルム、2は正極集電体、3は電解液
保持体、4は正極活物質、5は負極活物質、6は溶着
部、7は負極集電体FIG. 1 is a sectional view of a sealed lead-acid battery showing an embodiment of the present invention, FIG. 2 is a plan view showing a positive electrode plate in the embodiment of the present invention, and FIG. 3 is an active material at the time of discharging 0.1 C. Utilization comparison chart,
FIG. 4 is a comparison diagram of active material utilization rates during 2C discharge. 1, 1'is a resin film, 2 is a positive electrode current collector, 3 is an electrolytic solution holder, 4 is a positive electrode active material, 5 is a negative electrode active material, 6 is a welded portion, 7 is a negative electrode current collector
Claims (1)
に負極活物質にそれぞれ多数の角形状または丸形状に形
成させ、各極活物質間に電解液保持体を配した正、負極
板が、電解液保持体を介して積層され、電解液と共に密
封されたことを特徴とする密閉形鉛蓄電池。1. A positive electrode active material is formed on a positive electrode current collector, and the negative electrode active material is formed on the negative electrode current collector in a number of angular shapes or round shapes, and an electrolyte solution holder is arranged between the respective positive electrode active materials. A sealed lead-acid battery in which positive and negative electrode plates are laminated via an electrolytic solution holder and sealed together with the electrolytic solution.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63211524A JPH0624143B2 (en) | 1988-08-25 | 1988-08-25 | Sealed lead acid battery |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63211524A JPH0624143B2 (en) | 1988-08-25 | 1988-08-25 | Sealed lead acid battery |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0260066A JPH0260066A (en) | 1990-02-28 |
| JPH0624143B2 true JPH0624143B2 (en) | 1994-03-30 |
Family
ID=16607325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63211524A Expired - Lifetime JPH0624143B2 (en) | 1988-08-25 | 1988-08-25 | Sealed lead acid battery |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0624143B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2782802B2 (en) * | 1989-06-27 | 1998-08-06 | 新神戸電機株式会社 | Sealed lead-acid battery |
-
1988
- 1988-08-25 JP JP63211524A patent/JPH0624143B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0260066A (en) | 1990-02-28 |
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