JPH0682547B2 - Battery pack - Google Patents
Battery packInfo
- Publication number
- JPH0682547B2 JPH0682547B2 JP62157374A JP15737487A JPH0682547B2 JP H0682547 B2 JPH0682547 B2 JP H0682547B2 JP 62157374 A JP62157374 A JP 62157374A JP 15737487 A JP15737487 A JP 15737487A JP H0682547 B2 JPH0682547 B2 JP H0682547B2
- Authority
- JP
- Japan
- Prior art keywords
- battery
- case
- battery pack
- styrene
- weight
- 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 - Fee Related
Links
Classifications
-
- 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
- H01M50/20—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders
- H01M50/233—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders characterised by physical properties of casings or racks, e.g. dimensions
- H01M50/24—Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders characterised by physical properties of casings or racks, e.g. dimensions adapted for protecting batteries from their environment, e.g. from corrosion
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/18—Cells with non-aqueous electrolyte with solid electrolyte
- H01M6/20—Cells with non-aqueous electrolyte with solid electrolyte working at high temperature
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Sealing Battery Cases Or Jackets (AREA)
- Battery Mounting, Suspending (AREA)
Description
【発明の詳細な説明】 イ 産業上の利用分野 本発明は少くとも一つの有機電解液電池と、該電池を収
納する電池ケースとを備える電池パツクに関するもので
ある。TECHNICAL FIELD The present invention relates to a battery pack including at least one organic electrolyte battery and a battery case accommodating the battery.
ロ 従来の技術 有機電解液電池はリチウム、ナトリウムなどの軽金属を
負極活物質とし、二酸化マンガン、フツ化炭素などを正
極活物質とし、有機溶媒と溶質とからなる有機電解液を
用いるものであって、高エネルギー密度を有し且自己放
電が少ないという利点を有するものである。そしてこの
電池を電池ケースに収納し電池パツクとして携帯用機器
の電源やメモリーバツクアツプ用電源に有用されてい
る。(B) Conventional technology Organic electrolyte batteries use light metals such as lithium and sodium as the negative electrode active material, manganese dioxide, carbon fluoride, etc. as the positive electrode active material, and use an organic electrolyte solution composed of an organic solvent and a solute. However, it has the advantages of high energy density and little self-discharge. The battery is housed in a battery case and is used as a battery pack for the power supply of portable devices and the power supply for memory backup.
ところで最近の電池技術の目覚しい向上により、電池使
用最高温度として100℃程度の高温に設定して電池設計
が行なわれる場合があり、それに伴ない電池を収納する
ケース自体も耐熱性の改善が要求されている。By the way, due to recent remarkable improvements in battery technology, battery design may be carried out by setting the maximum battery usage temperature to a high temperature of about 100 ° C, and accompanying this, improvement in heat resistance is required for the case itself that houses the battery. ing.
従来のケースは例えばABS(アクリロニトリルスチレン
ブタジエン共重合体)、PS(ポリスチレン)、PC(ポリ
カーボネート)などで形成されていた。The conventional case is formed of, for example, ABS (acrylonitrile-styrene-butadiene copolymer), PS (polystyrene), PC (polycarbonate), or the like.
ハ 発明が解決しようとする問題点 前述せるABS、PSは耐熱温度〔UL温度インデツクス:Unde
rwriters Laboratories(米国)で指定されている最高
連続使用温度〕が60〜80℃と電池使用最高温度よりも低
く、本来電池を保護するためのものであるケースの品質
としては不充分である。又PCは耐熱温度が120℃と高く
充分と云えるが、耐有機電解液性に難があり、そのため
ケース内で有機電解液が電池より漏出した場合、有機電
解液と接するケースの部分は侵食され膨潤、溶解或いは
溶剤亀裂を生じ、周辺機器に悪影響を与える。尚、AB
S、PSも耐有機電解液性についてはPCの場合と同様のこ
とが云える。C. Problems to be solved by the invention ABS and PS described above are heat resistant (UL temperature index: Unde
The maximum continuous operating temperature specified by rwriters Laboratories (USA)] is 60 to 80 ° C, which is lower than the maximum operating temperature of the battery, which is not sufficient as the quality of the case originally intended to protect the battery. Although PC can be said to have a high heat resistance temperature of 120 ° C, which is sufficient, the resistance to organic electrolytic solution is poor, so if the organic electrolytic solution leaks from the battery inside the case, the part of the case that comes in contact with the organic electrolytic solution will be eroded. It causes swelling, dissolution or solvent cracking, which adversely affects peripheral equipment. Incidentally, AB
It can be said that S and PS have the same resistance to organic electrolyte as those of PC.
ニ 問題点を解決するための手段 電池ケース材料としてスチレンを10〜40重量%含有する
変性ポリフエニレンオキシド樹脂を用いる。D Means for solving the problem A modified polyphenylene oxide resin containing 10 to 40% by weight of styrene is used as a battery case material.
ホ 作用 変性ポリフエニレンオキシド樹脂中のスチレンの添加量
に対する耐熱温度、スパイラル流動長さ及び電解液浸漬
試験による重量変化率を第1図に示す。E. Actions Figure 1 shows the heat resistance temperature, the spiral flow length, and the weight change rate by the electrolytic solution immersion test with respect to the amount of styrene added to the modified polyphenylene oxide resin.
第1図よりスチレンの添加量が40重量%を越えると耐熱
温度は100℃以下となり、電池ケースとしては前述した
ように不適当であると共に、電解液浸漬実験において重
量変化率が急激に上昇し始め浸食が大きくなることがわ
かる。As shown in Fig. 1, when the amount of styrene added exceeds 40% by weight, the heat-resistant temperature becomes 100 ° C or less, which is unsuitable as a battery case as described above, and the weight change rate rapidly increases in the electrolyte immersion experiment. It can be seen that the erosion increases at the beginning.
一方、スチレンの添加量が10重量%より少ないとスパイ
ラル流動長さが短くなり射出成形加工性が悪くなって成
形加工が困難となる。On the other hand, if the addition amount of styrene is less than 10% by weight, the spiral flow length becomes short, the injection molding processability deteriorates, and the molding process becomes difficult.
尚、重量変化率はジメトキシエタンとテトラヒドロフラ
ンとの混合溶媒中に60℃で7日間材料を浸漬し、浸漬前
後の重量変化を示すものである。又、スパイラル流動長
さはスパイラル状に溝を形成した金型を60℃に保ち、シ
リンダ温度240℃、射出圧力1320kg/cm2の条件で樹脂を
前記スパイラル状溝に射出し樹脂の流れた距離を示し、
距離が長いほど成形性が良好である。The weight change rate indicates the weight change before and after immersion of the material in a mixed solvent of dimethoxyethane and tetrahydrofuran at 60 ° C. for 7 days. The spiral flow length is maintained at 60 ° C in a mold with spiral grooves, and the resin is injected into the spiral grooves under the conditions of a cylinder temperature of 240 ° C and an injection pressure of 1320kg / cm 2 , and the distance the resin flows. Indicates
The longer the distance, the better the moldability.
第1図からスチレンの添加量としては10〜40重量%の範
囲が好ましいことが理解される。It is understood from FIG. 1 that the addition amount of styrene is preferably in the range of 10 to 40% by weight.
ヘ 実施例 第1表はポリフエニレンオキシドにスチレンを25重量%
添加し共重合体化した本発明における変性ポリフエニレ
ンオキシド(変性PPO)の試験片と、従来のABS、PS及び
PCの各試験片との電解液浸漬試験による重量変化率及び
外観状態を比較して示す。尚、この場合の電解液浸漬試
験は有機電解液としてプロピレンカーボネートとジメト
キシエタンとの混合溶媒に過塩素酸リチウムを溶解した
ものを用い、20℃で10日間浸漬するという条件で行なつ
た。F. Examples Table 1 shows polyphenylene oxide containing 25% by weight of styrene.
A test piece of the modified polyphenylene oxide (modified PPO) of the present invention, which was added and copolymerized, and conventional ABS, PS and
The rate of change in weight and the appearance state of each test piece of PC in an electrolyte immersion test are shown in comparison. In this case, the electrolytic solution immersion test was carried out under the conditions of immersion at 20 ° C. for 10 days using an organic electrolytic solution prepared by dissolving lithium perchlorate in a mixed solvent of propylene carbonate and dimethoxyethane.
第1表より変性PPOは耐有機電解液特性に優れているこ
とがわかる。 It can be seen from Table 1 that the modified PPO has excellent organic electrolyte resistance.
第2図は本発明による電池パツクの分解斜視図を示し、
(1)(2)はスチレンを25重量%含有する変性ポリフ
エニレンオキシドからなる二つ割電池ケースであり、一
方のケース(1)の上端面には一対の切欠部(3)
(3)が形成されており、他方のケース(2)には前記
切欠部(3)(3)に嵌合する突片(4)(4)が形成
されている。FIG. 2 is an exploded perspective view of the battery pack according to the present invention,
(1) and (2) are split battery cases made of modified polyphenylene oxide containing 25% by weight of styrene, and one case (1) has a pair of notches (3) at the upper end surface.
(3) is formed, and the other case (2) is provided with protrusions (4) and (4) that fit into the cutouts (3) and (3).
電池パツク組立に際しては接続片(5)により直列接続
した一対の有機電解液電池(6)(6)を一方のケース
(1)の凹所(7)に収納した後、端子金具(8)
(8)の一端(8)′(8)′を対応電池の端子部にス
ポツト溶接する。そして各端子金具(8)(8)を一方
のケース(1)の上端面に設けた切欠部(3)(3)及
び側面に設けた透孔(9)(9)によつて係止、固定し
た後、他方のケース(2)を被せ二つ割ケースの接合部
を超音波溶接して完成電池パツクを得る。尚、一対の電
池(6)(6)は短絡を阻止するために少くとも一方の
電池を絶縁チユーブで被覆している。When assembling the battery pack, the pair of organic electrolyte batteries (6) and (6) connected in series by the connecting piece (5) are housed in the recess (7) of the one case (1), and then the terminal fitting (8).
One end (8) '(8)' of (8) is spot welded to the terminal portion of the corresponding battery. Then, the terminal fittings (8) and (8) are locked by notches (3) and (3) provided on the upper end surface of one case (1) and through holes (9) and (9) provided on the side surfaces, After fixing, the other case (2) is covered and the joint portion of the split case is ultrasonically welded to obtain a completed battery pack. Incidentally, the pair of batteries (6) and (6) have at least one of the batteries covered with an insulating tube in order to prevent a short circuit.
ト 発明の効果 上述した如く、本発明によれば電池ケースの材料に用い
たスチレン10〜40重量%含有の変性ポリフエナレンオキ
シドが有機電解液に対して極めて安定であるので異常時
に電池から有機電解液が漏出してもケースが溶解した
り、膨潤して亀裂を生じると云つた不都合がなく周辺機
器への損傷を最小限度に抑えることができると共に、耐
熱性も温度インデツクスで100℃以上を有するので高温
条件下での使用の場合においてもケースの劣化がなく安
定性に優れた電池パツクを得ることができるものであ
り、その工業的価値は極めて大である。Effect of the Invention As described above, according to the present invention, the modified polyphenylene oxide containing 10 to 40% by weight of styrene used as the material of the battery case is extremely stable to the organic electrolytic solution, so that it is possible to remove the organic compound from the battery during abnormal conditions. Even if the electrolyte leaks out, there is no inconvenience that the case dissolves or swells and cracks, and it is possible to minimize damage to peripheral equipment, and the heat resistance is 100 ° C or more in temperature index. Since it has a high temperature, it is possible to obtain a battery pack excellent in stability without deterioration of the case even when used under high temperature conditions, and its industrial value is extremely large.
第1図は変性ポリフエニレンオキシドへのスチレンの添
加量と諸物性の関係を示す図、第2図は電池パツクの分
解斜視図である。 (1)(2)……二つ割電池ケース、(3)(3)……
切欠部、(4)(4)……突片、(5)……接続片、
(6)(6)……有機電解液電池、(8)(8)……端
子金具、(9)(9)……透孔。FIG. 1 is a diagram showing the relationship between the amount of styrene added to the modified polyphenylene oxide and various physical properties, and FIG. 2 is an exploded perspective view of the battery pack. (1) (2) …… Battery case, (3) (3) ……
Notch, (4) (4) ... Projection piece, (5) ... Connection piece,
(6) (6) ... organic electrolyte battery, (8) (8) ... terminal fittings, (9) (9) ... through holes.
Claims (1)
を収納する電池ケースとを備え、前記ケースがスチレン
を10〜40重量%含有する変性ポリフエニレンオキシド樹
脂からなることを特徴とする電池パツク。1. At least one organic electrolyte battery and a battery case accommodating the battery, wherein the case is made of a modified polyphenylene oxide resin containing 10 to 40% by weight of styrene. Battery pack to be used.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62157374A JPH0682547B2 (en) | 1987-06-24 | 1987-06-24 | Battery pack |
KR1019880007682A KR890001213A (en) | 1987-06-24 | 1988-06-23 | Battery pack |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62157374A JPH0682547B2 (en) | 1987-06-24 | 1987-06-24 | Battery pack |
Publications (3)
Publication Number | Publication Date |
---|---|
JPH012250A JPH012250A (en) | 1989-01-06 |
JPS642250A JPS642250A (en) | 1989-01-06 |
JPH0682547B2 true JPH0682547B2 (en) | 1994-10-19 |
Family
ID=15648260
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62157374A Expired - Fee Related JPH0682547B2 (en) | 1987-06-24 | 1987-06-24 | Battery pack |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPH0682547B2 (en) |
KR (1) | KR890001213A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5709963A (en) * | 1996-07-25 | 1998-01-20 | Daewoo Electronics Co., Inc. | Battery pack |
US5744260A (en) * | 1996-07-25 | 1998-04-28 | Daewoo Electronics Co., Ltd. | Battery pack |
FR2762716B1 (en) * | 1997-04-28 | 1999-05-28 | Alsthom Cge Alcatel | DEVICE FOR ASSEMBLING BATTERIES OF ELECTROCHEMICAL GENERATORS |
-
1987
- 1987-06-24 JP JP62157374A patent/JPH0682547B2/en not_active Expired - Fee Related
-
1988
- 1988-06-23 KR KR1019880007682A patent/KR890001213A/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
KR890001213A (en) | 1989-03-18 |
JPS642250A (en) | 1989-01-06 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |