JP4488696B2 - Lead storage battery inspection equipment - Google Patents
Lead storage battery inspection equipment Download PDFInfo
- Publication number
- JP4488696B2 JP4488696B2 JP2003186757A JP2003186757A JP4488696B2 JP 4488696 B2 JP4488696 B2 JP 4488696B2 JP 2003186757 A JP2003186757 A JP 2003186757A JP 2003186757 A JP2003186757 A JP 2003186757A JP 4488696 B2 JP4488696 B2 JP 4488696B2
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- Prior art keywords
- specific gravity
- storage battery
- electrolytic solution
- lead storage
- lead
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- 238000007689 inspection Methods 0.000 title claims description 12
- 230000005484 gravity Effects 0.000 claims description 54
- 239000008151 electrolyte solution Substances 0.000 claims description 45
- 230000015572 biosynthetic process Effects 0.000 claims description 21
- 239000003792 electrolyte Substances 0.000 claims description 19
- 239000002253 acid Substances 0.000 claims description 6
- 238000005259 measurement Methods 0.000 claims description 4
- 238000001514 detection method Methods 0.000 description 16
- 239000011149 active material Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 8
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- YADSGOSSYOOKMP-UHFFFAOYSA-N dioxolead Chemical compound O=[Pb]=O YADSGOSSYOOKMP-UHFFFAOYSA-N 0.000 description 4
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 229910000464 lead oxide Inorganic materials 0.000 description 3
- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 3
- 229910000978 Pb alloy Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000004904 shortening Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
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Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R31/00—Arrangements for testing electric properties; Arrangements for locating electric faults; Arrangements for electrical testing characterised by what is being tested not provided for elsewhere
- G01R31/36—Arrangements for testing, measuring or monitoring the electrical condition of accumulators or electric batteries, e.g. capacity or state of charge [SoC]
- G01R31/378—Arrangements for testing, measuring or monitoring the electrical condition of accumulators or electric batteries, e.g. capacity or state of charge [SoC] specially adapted for the type of battery or accumulator
- G01R31/379—Arrangements for testing, measuring or monitoring the electrical condition of accumulators or electric batteries, e.g. capacity or state of charge [SoC] specially adapted for the type of battery or accumulator for lead-acid batteries
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01R—MEASURING ELECTRIC VARIABLES; MEASURING MAGNETIC VARIABLES
- G01R31/00—Arrangements for testing electric properties; Arrangements for locating electric faults; Arrangements for electrical testing characterised by what is being tested not provided for elsewhere
- G01R31/50—Testing of electric apparatus, lines, cables or components for short-circuits, continuity, leakage current or incorrect line connections
- G01R31/52—Testing for short-circuits, leakage current or ground faults
-
- 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
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Secondary Cells (AREA)
Description
【0001】
【発明の属する技術分野】
本発明は、電槽化成後の蓄電池の短絡状態を検査する蓄電池の検査装置に関する。
【0002】
【従来の技術】
一般に、鉛蓄電池は、硫酸電解液中に正極と負極を配置したセルが複数個直列接続された構造となっている。また、正極は鉛合金格子基板に過酸化鉛の活物質が充填されたものであり、負極は鉛合金格子基板に海綿状金属鉛の活物質が充填されたものである。なお、一般に正極の活物質である過酸化鉛および負極の活物質である海綿状金属鉛は、それぞれ酸化鉛および硫酸鉛を主原料としており、電槽化成工程を経て、正極の活物質は過酸化鉛となり、負極の活物質は海綿状金属鉛となる。
【0003】
ところで、上記のような鉛蓄電池の電槽化成工程においては、極板間の短絡が発生することがある。この短絡には、両極間に起電力が発生しなくなる程度の重度な短絡と、電槽化成後に数日間放置して電圧の低下がわかる程度の軽度な短絡がある。
【0004】
鉛蓄電池の短絡を検知するための方法として、電槽化成前の極板間に電圧をかける方法(特許文献1参照)、充電中に各セル内で発生するガスの圧力又は量を計測する方法(特許文献2参照)などが知られている。また、特許文献2には、鉛蓄電池の充電完了後に、両極端子間のオープン電圧を測定する方法や電解液比重を測定する方法なども従来技術として記載されている。
【0005】
【特許文献1】
特開平4−138674号公報
【特許文献2】
特開昭57−196481号公報
【0006】
【発明が解決しようとする課題】
しかし、特許文献1に記載された技術には、電槽化成後の極板間の短絡状態を検知することができないという問題点がある。また、特許文献2に記載された技術には、ガスの圧力や量を正確に計測することが難しいという問題点がある。
【0007】
そこで、本発明は、電槽化成後の極板間の短絡状態を短時間で検知することが可能な鉛蓄電池の検査装置を提供することを目的とする。
【0008】
【課題を解決するための手段】
請求項1の発明は、電槽化成後の電解液の比重が所定の値となるように、電槽化成前の電解液の比重を小さく設定し、電槽化成後の鉛蓄電池の電解液の比重を計測することにより前記鉛蓄電池の各セル内の短絡状態を検査する鉛蓄電池の検査装置において、前記鉛蓄電池の電解液の比重を計測する電解液比重計測手段を前記鉛蓄電池のセル数と同数備え、該電解液比重計測手段に連結され該電解液比重計測手段に前記鉛蓄電池内の電解液を導入する電解液導入手段を備え、該電解液導入手段は、前記鉛蓄電池内の電解液を各電解液比重計測手段へ一括して導入する機能を有することを特徴とする。
【0009】
【発明の実施の形態】
以下、本発明の実施形態を説明する。
【0010】
図1は、本発明の実施形態である鉛蓄電池の検査装置を蓄電池に取り付けた状態を示す概略側面図であり、図2は図1に対応する概略正面図であり、図3および図4は図1に対応する概略上面図である。
【0011】
図1〜図4において、1は鉛蓄電池であって、11は端子、12はセルである。鉛蓄電池1はその内部でセル12が6個直列に接続されている。
【0012】
また、図1〜図4において、2は電解液比重計測手段としての比重検出装置であって、比重検出装置2はセル12の数と同数であり、各セル12の電解液の比重を検出することができるようになっている。比重検出装置2は、蓄電池1の各セル12と比重検出装置2とを連結する連結管21、比重検出装置2内で上下に移動可能な比重計22を備えている。なお、23は鉛蓄電池1から吸い上げられた電解液、24は電解液23の液面である。
【0013】
また、図1〜図4において、3は比重検出装置2に電解液を導入する電解液導入手段としての電解液導入装置、4は比重検出装置2と電解液導入装置3とを連結する連結管である。
【0014】
電解液導入装置3は、比重検出装置2と連結されたシリンダー31を備えている。シリンダー31は、往復運動するピストン軸31aと、ピストン軸31aのうちシリンダー31内側の一端にヘッド31bとを有している。シリンダー31は、ヘッド31bのピストン軸31a側において外気に開放されている。
【0015】
ここで、図3に例示されるように、電解液導入装置3のシリンダー31の数は比重検出装置2の数と同数であって各シリンダー31はそれぞれ比重検出装置2に1対1で接続されているものであってもよく、図4に例示されるように、1本のシリンダー31が連結管4を通して各比重検出装置2に一括して接続されているものであってもよい。
【0016】
また、電解液導入装置3は、シリンダー31のピストン軸31aを動作させるための駆動用シリンダー32を備えており、駆動用シリンダー32は往復運動するピストン軸32aと、ピストン軸32aのうち駆動用シリンダー32内側の一端にヘッド32bとを有している。駆動用シリンダー32には、電磁弁33が設けられており、ピストン軸32aを空気等により駆動する。ピストン軸31aとピストン軸32aとは、連結体34で連結されている。ここで、図1および図3に例示されるように、各ピストン軸31aは連結体34を介して1本のピストン軸32aに接続されていてもよく、図4に例示されるように、1本のピストン軸31が連結体34を介して1本のピストン軸32aに接続されていてもよい。
【0017】
以下、図1および図3を用いて、電解液導入装置3の動作状態の一例について説明する。まず、電磁弁33により駆動用シリンダー32が動作し、ピストン軸32aが図1の右側(図3の上側)に動く。このピストン軸32aは、連結体34を介して各ピストン軸31aを図1の右側(図3の上側)に動かし、各ヘッド31bが各シリンダー31内を図1の右側(図3の上側)に動く。
【0018】
次に、図1および図2を用いて、比重検出装置2における電解液23の比重の検出について説明する。上述のように各ヘッド31bが動くことにより、比重検出装置2内の空気が図1および図2の上側に引っ張られ、鉛蓄電池1の各セル12内の電解液23が図1および図2の液面24まで引っ張られる。そして、比重検出装置2内の比重計22が電解液に所定の目盛位置で浮き、これを目視等により検知することで、電解液23の比重を検出することができる。
【0019】
以上、本発明の実施形態である鉛蓄電池の検査装置の一例を説明したが、本発明の実施形態はこれに限られるものではない。
【0020】
また、本発明の実施形態である鉛蓄電池の検査装置を用いて、両極間に起電力が発生しなくなる程度の重度な短絡のほか、電槽化成後に数日間放置して電圧の低下がわかる程度の軽度な短絡についても検出することができる。以下、その一例を説明する。
【0021】
電槽化成前の正極の活物質である過酸化鉛および負極の活物質である海綿状金属鉛は、それぞれ酸化鉛および硫酸鉛を主原料としており、電槽化成工程を経て、正極の活物質は過酸化鉛となり、負極の活物質は海綿状金属鉛となる。この電槽化成工程において、活物質中の硫酸分が電解液中に放出されるため、電槽化成後の電解液の比重が所定の値となるように、電槽化成前の電解液の比重を小さく設定することで、電解液の交換などをする必要がなくすことができる。
【0022】
電槽化成前の電解液の比重を小さく設定しておくと、極板間に重度の短絡が発生している場合には電槽化成後の電解液の比重がほとんど変化せず、また、極板間に軽度の短絡が発生している場合には電槽化成後の電解液の比重の変化の割合が小さくなるため、電槽化成後の電解液の比重を検出することにより、極板間の短絡を検知することができる。
【0023】
実際に、電槽化成前の電解液の比重を1.230(20℃、以下同様)、電槽化成後の電解液の比重を1.280となるように両極の活物質材料を選定したところ、極板間に重度の短絡が発生している場合の電槽化成後の電解液の比重は1.230〜1.250、極板間に軽度の短絡が発生している場合には電槽化成後の電解液の比重は1.260〜1.270であり、本発明の実施形態である鉛蓄電池の検査装置を用いて極板間の短絡を検知することが可能であった。
【0024】
また、電槽化成後の電解液の比重が1.260〜1.270である鉛蓄電池を48時間放置したところ、いずれも蓄電池電圧が12.50〜12.70Vまで低下しており、軽度の短絡が発生していたことが確認された。
【0025】
また、本発明の実施形態である鉛蓄電池の検査装置を用いて鉛蓄電池の短絡状態を検査するための所要時間は、図1〜図4に例示された状態で1回の測定で数秒〜10数秒であり、鉛蓄電池の短絡をその度合いにかかわらず短時間で検知することができ、特に軽度の短絡を検知するための時間短縮効果が大きくなる。
【0026】
【発明の効果】
以上のとおり、本発明によれば、鉛蓄電池の電解液の比重を計測する電解液比重計測手段を鉛蓄電池のセル数と同数備え、電解液比重計測手段に連結され電解液比重計測手段に鉛蓄電池内の電解液を導入する電解液導入手段を備え、電解液導入手段は、鉛蓄電池内の電解液を各電解液比重計測手段へ一括して導入する機能を有しているため、電槽化成後の鉛蓄電池の短絡を短時間で検知することができ、特に軽度の短絡を検知するための時間短縮効果が大きくなる。
【図面の簡単な説明】
【図1】 本発明の実施形態である鉛蓄電池の検査装置を蓄電池に取り付けた状態の一例を示す概略側面図である。
【図2】 図1に対応する概略正面図である。
【図3】 図1に対応する概略上面図の第1例である。
【図4】 図1に対応する概略上面図の第2例である。
【符号の説明】
1 鉛蓄電池
2 比重検出装置
3 電解液導入装置
4 連結管
11 端子
12 セル
21 連結管
22 比重計
23 電解液
24 液面
31 シリンダー
31a、32a ピストン軸
31b、32b ヘッド
32 駆動用シリンダー
33 電磁弁
34 連結体[0001]
BACKGROUND OF THE INVENTION
The present invention relates to a storage battery inspection device that inspects a short circuit state of a storage battery after battery case formation.
[0002]
[Prior art]
In general, a lead storage battery has a structure in which a plurality of cells in which a positive electrode and a negative electrode are arranged in a sulfuric acid electrolyte solution are connected in series. The positive electrode is a lead alloy lattice substrate filled with an active material of lead peroxide, and the negative electrode is a lead alloy lattice substrate filled with an active material of spongy metallic lead. In general, lead peroxide as the active material of the positive electrode and spongy metal lead as the active material of the negative electrode are mainly made of lead oxide and lead sulfate, respectively. It becomes lead oxide, and the active material of the negative electrode becomes spongy metallic lead.
[0003]
By the way, in the battery case formation process of the above lead acid battery, the short circuit between electrode plates may generate | occur | produce. This short circuit includes a severe short circuit that does not generate an electromotive force between the two electrodes, and a short circuit that can be left for several days after forming the battery case to show a voltage drop.
[0004]
As a method for detecting a short circuit of a lead storage battery, a method of applying a voltage between electrode plates before battery case formation (see Patent Document 1), a method of measuring the pressure or amount of gas generated in each cell during charging (See Patent Document 2) and the like.
[0005]
[Patent Document 1]
Japanese Patent Laid-Open No. 4-138673 [Patent Document 2]
Japanese Patent Laid-Open No. 57-196481 [0006]
[Problems to be solved by the invention]
However, the technique described in
[0007]
Then, an object of this invention is to provide the inspection apparatus of the lead storage battery which can detect the short circuit state between the electrode plates after battery case formation in a short time.
[0008]
[Means for Solving the Problems]
The invention of
[0009]
DETAILED DESCRIPTION OF THE INVENTION
Embodiments of the present invention will be described below.
[0010]
FIG. 1 is a schematic side view showing a state where an inspection apparatus for a lead storage battery according to an embodiment of the present invention is attached to a storage battery, FIG. 2 is a schematic front view corresponding to FIG. 1, and FIGS. FIG. 2 is a schematic top view corresponding to FIG. 1.
[0011]
1 to 4, 1 is a lead storage battery, 11 is a terminal, and 12 is a cell. The
[0012]
1 to 4,
[0013]
1 to 4,
[0014]
The electrolytic
[0015]
Here, as illustrated in FIG. 3, the number of
[0016]
The
[0017]
Hereinafter, an example of the operation state of the electrolytic
[0018]
Next, detection of the specific gravity of the
[0019]
As mentioned above, although an example of the inspection apparatus of the lead storage battery which is embodiment of this invention was demonstrated, embodiment of this invention is not restricted to this.
[0020]
In addition to using a lead storage battery inspection device according to an embodiment of the present invention, in addition to a severe short circuit that does not generate an electromotive force between the two electrodes, it can be left to stand for several days after the battery is formed, and a decrease in voltage can be seen. Even a slight short circuit can be detected. An example will be described below.
[0021]
Lead peroxide, which is the active material of the positive electrode before the formation of the battery case, and spongy metal lead, which is the active material of the negative electrode, are mainly made of lead oxide and lead sulfate. Becomes lead peroxide, and the active material of the negative electrode becomes spongy metallic lead. In this battery case formation step, the sulfuric acid content in the active material is released into the electrolyte solution. Therefore, the specific gravity of the electrolyte solution before battery case formation is such that the specific gravity of the electrolyte solution after battery case formation becomes a predetermined value. By setting the value small, it is possible to eliminate the need to exchange the electrolyte.
[0022]
If the specific gravity of the electrolyte before battery case formation is set small, the specific gravity of the electrolyte after battery case formation will hardly change if a severe short circuit occurs between the electrode plates. When a slight short circuit occurs between the plates, the rate of change in the specific gravity of the electrolytic solution after battery case formation becomes small, so by detecting the specific gravity of the electrolytic solution after battery case formation, Can be detected.
[0023]
Actually, the active material of both electrodes was selected so that the specific gravity of the electrolytic solution before forming the battery case was 1.230 (20 ° C., the same applies hereinafter) and the specific gravity of the electrolytic solution after forming the battery case was 1.280. The specific gravity of the electrolyte after the formation of the battery case when a severe short circuit occurs between the electrode plates is 1.230 to 1.250, and the battery case when a slight short circuit occurs between the electrode plates The specific gravity of the electrolytic solution after chemical conversion was 1.260 to 1.270, and it was possible to detect a short circuit between the electrode plates using the lead storage battery inspection device according to the embodiment of the present invention.
[0024]
Moreover, when the lead acid battery whose specific gravity of the electrolyte solution after battery case formation is 1.260-1.270 was left for 48 hours, all the battery voltage fell to 12.50-12.70V, and it was mild. It was confirmed that a short circuit had occurred.
[0025]
Moreover, the time required to test | inspect the short circuit state of lead acid battery using the test | inspection apparatus of lead acid battery which is embodiment of this invention is several seconds-10 by one measurement in the state illustrated in FIGS. It is several seconds, and a short circuit of the lead storage battery can be detected in a short time regardless of the degree thereof, and the time shortening effect for detecting a light short circuit is particularly great.
[0026]
【The invention's effect】
As described above, according to the present invention, the electrolytic solution specific gravity measuring means for measuring the specific gravity of the electrolytic solution of the lead storage battery is provided in the same number as the number of cells of the lead storage battery, and connected to the electrolytic solution specific gravity measuring means. An electrolytic solution introducing means for introducing the electrolytic solution in the storage battery is provided, and the electrolytic solution introducing means has a function of collectively introducing the electrolytic solution in the lead storage battery to each electrolytic solution specific gravity measuring means. The short circuit of the lead storage battery after chemical conversion can be detected in a short time, and the effect of shortening the time for detecting a light short circuit in particular is increased.
[Brief description of the drawings]
FIG. 1 is a schematic side view showing an example of a state in which a lead storage battery inspection device according to an embodiment of the present invention is attached to a storage battery.
FIG. 2 is a schematic front view corresponding to FIG. 1;
FIG. 3 is a first example of a schematic top view corresponding to FIG. 1;
FIG. 4 is a second example of a schematic top view corresponding to FIG. 1;
[Explanation of symbols]
DESCRIPTION OF
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Priority Applications (1)
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JPH02210771A (en) * | 1989-02-09 | 1990-08-22 | Japan Storage Battery Co Ltd | Sealed type lead storage battery |
JPH0945379A (en) * | 1995-04-22 | 1997-02-14 | Kenichi Fujita | Electrolyte for lead-acid battery, lead-acid battery using it, and reproduction possibility judging method of lead-acid battery |
JP2002110217A (en) * | 2000-09-27 | 2002-04-12 | Japan Storage Battery Co Ltd | Battery inspection method |
JP2003168472A (en) * | 2001-11-29 | 2003-06-13 | Yuasa Corp | Formation method for battery jar of control valve type lead-acid battery |
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FR2020290A1 (en) * | 1968-10-10 | 1970-07-10 | Gould National Batteries Inc |
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JPH02210771A (en) * | 1989-02-09 | 1990-08-22 | Japan Storage Battery Co Ltd | Sealed type lead storage battery |
JPH0945379A (en) * | 1995-04-22 | 1997-02-14 | Kenichi Fujita | Electrolyte for lead-acid battery, lead-acid battery using it, and reproduction possibility judging method of lead-acid battery |
JP2002110217A (en) * | 2000-09-27 | 2002-04-12 | Japan Storage Battery Co Ltd | Battery inspection method |
JP2003168472A (en) * | 2001-11-29 | 2003-06-13 | Yuasa Corp | Formation method for battery jar of control valve type lead-acid battery |
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