JPH0793131B2 - Battery - Google Patents
BatteryInfo
- Publication number
- JPH0793131B2 JPH0793131B2 JP1058310A JP5831089A JPH0793131B2 JP H0793131 B2 JPH0793131 B2 JP H0793131B2 JP 1058310 A JP1058310 A JP 1058310A JP 5831089 A JP5831089 A JP 5831089A JP H0793131 B2 JPH0793131 B2 JP H0793131B2
- Authority
- JP
- Japan
- Prior art keywords
- resin
- battery
- curable resin
- parts
- 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
-
- 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
- Sealing Battery Cases Or Jackets (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は、電池の端子露出面に紫外線硬化型の樹脂を充
填して構成される電池に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a battery configured by filling a terminal exposed surface of the battery with an ultraviolet curable resin.
従来の技術 従来より、電池の正極端子、および負極端子の同一面に
露出する端子間部分には、絶縁性部材を介在させて外部
からの金属部片の接触による短絡、あるいは結露などに
よる液絡現象の防止が図られていた。特にリチウム電
池、アルカリ電池のような高出力電池である場合、短絡
した時には大電流が流れ、電池自身が発熱して、電池封
口部分が変形したり、内蔵電解液が漏出し使用機器を損
傷させたり、あるいは水分などが両極端子間に介在して
液絡状態になった時、リチウム電池のような3V級の電位
を示す電池にあっては水の電気分解が起こり、端子金属
を腐食させるなどの問題があった。これらの問題を解決
する絶縁部材としては、従来より金属との密着性,接着
性に優れる高分子材料が用いられてきた。これらの接着
剤は溶剤可溶型、あるいは二液混合型の接着組成物が主
なものであるが、硬化するまでに長時間を要したり、溶
剤可溶型のものにあっては生産ラインの中で溶剤を飛散
させる工程が必要となり、電池製造コストが高くなるも
のであった。反面紫外線硬化型の接着組成物は主成分と
して、分子中に二重結合などの反応基を有した光重合性
プレポリマー,希釈剤としての光重合性モノマー、なら
びに光反応開始剤からなる無溶剤型接着組成物であり紫
外線を照射することにより瞬時に接着硬化するため多用
されつつある。2. Description of the Related Art Conventionally, a positive electrode terminal of a battery and a negative electrode terminal exposed on the same surface between the terminals have an insulating member interposed between them to cause a short circuit due to contact with a metal piece from the outside or a liquid junction due to dew condensation. It was intended to prevent the phenomenon. Especially in the case of high output batteries such as lithium batteries and alkaline batteries, when a short circuit occurs, a large current flows, the battery itself generates heat, the battery sealing part is deformed, and the built-in electrolyte leaks out and damages the equipment used. Or, when water or the like exists between both terminals and becomes a liquid junction, electrolysis of water occurs in a battery showing a potential of 3V class such as a lithium battery, and the terminal metal is corroded. There was a problem. As an insulating member that solves these problems, a polymer material having excellent adhesion and adhesion to a metal has been used conventionally. These adhesives are mainly solvent-soluble type or two-liquid mixed type adhesive compositions, but it takes a long time to cure, and solvent-soluble type adhesives have a production line. In this case, a step of scattering the solvent is required, which increases the battery manufacturing cost. On the other hand, a UV-curable adhesive composition is a solvent-free composition containing a photopolymerizable prepolymer having a reactive group such as a double bond in the molecule, a photopolymerizable monomer as a diluent, and a photoreaction initiator as main components. It is a mold-bonding composition and is being widely used because it is instantly cured by irradiation with ultraviolet rays.
発明が解決しようとする課題 紫外線硬化型樹脂の接着硬化反応は前述したように紫外
線を照射されることによって光重合性プレポリマーと光
重合性モノマーの重合反応が起こり接着硬化される。こ
のため樹脂の肉厚が厚い場合、具体的には0.3m/m以上の
ような肉厚の場合、光重合反応が樹脂の表面層から開始
されるため、樹脂の表面層と内部層において樹脂の硬化
速度,重合度が異なるため、硬化後の樹脂の内部に歪を
内包した状態で接着硬化反応が行なわれる。このように
樹脂の内部で歪を残存した状態で樹脂が絶縁性部材とし
て端子露出面に接着硬化した場合、電池保存中,使用中
における自然環境に起因する長期的な環境ストレス、あ
るいは短期的な熱衝撃等の人意的な環境ストレスによっ
て樹脂の表面に亀裂が発生し、絶縁性部材として用をな
さない状態になる場合が多々あった。DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention In the adhesive curing reaction of an ultraviolet curable resin, a polymerization reaction of a photopolymerizable prepolymer and a photopolymerizable monomer occurs by being irradiated with ultraviolet rays as described above, and the adhesive is cured. For this reason, when the resin has a large thickness, specifically, when it has a thickness of 0.3 m / m or more, the photopolymerization reaction is started from the surface layer of the resin, so that the resin in the surface layer and the inner layer of the resin Since the curing speed and the degree of polymerization of the resin are different, the adhesive curing reaction is carried out in the state where the strain is contained in the cured resin. When the resin adheres and cures to the exposed surface of the terminal as an insulating member while the strain remains inside the resin, long-term environmental stress caused by the natural environment during storage or use of the battery, or short-term environmental stress In many cases, the surface of the resin was cracked by human environmental stress such as thermal shock, so that the resin could not be used as an insulating member.
課題を解決するための手段 本発明は前述した問題点を樹脂素材について鋭意検討を
行なって解決したものであり、光重合性プレポリマーと
してウレタンアクリレート樹脂が20〜40重量部,光重合
性モノマーとしてアクリル樹脂が50〜80重量部からなる
紫外線硬化樹脂を用いることによって硬化後の内部歪が
小さく、耐クラック性に優れる絶縁性部材を電池の端子
露出部に介在させたものである。Means for Solving the Problems The present invention has been made by solving the above-mentioned problems by intensively studying a resin material, wherein a urethane acrylate resin as a photopolymerizable prepolymer is 20 to 40 parts by weight, and as a photopolymerizable monomer. By using an ultraviolet curable resin composed of 50 to 80 parts by weight of an acrylic resin, an insulating member having a small internal strain after curing and excellent in crack resistance is interposed in a terminal exposed portion of a battery.
作 用 前述のような配合の紫外線硬化型樹脂は、他の汎用的な
紫外線硬化型樹脂に比して硬化物がポリウレタン構造を
形成し、比較的粘稠なな弾力性のある硬化物を生成する
ため、硬化物の内部に発生する残存歪を吸収するような
作用を有するものと考えられる。The UV-curable resin with the above composition has a polyurethane structure as compared with other general-purpose UV-curable resins, and produces a relatively viscous and elastic cured product. Therefore, it is considered to have an action of absorbing the residual strain generated inside the cured product.
実施例 第1図は本発明の実施例を示す電池の要部断面図であ
る。Example FIG. 1 is a cross-sectional view of a main part of a battery showing an example of the present invention.
図中1は紫外線硬化型樹脂よりなる絶縁性部材であり、
これは正極の端子を兼ねる端子板2と、発電要素Aを内
蔵して負極の端子を兼ねる金属容器3と、双方の端子間
を電池内部で絶縁、ならびに内蔵発電要素Aが外部に漏
出するのを防止する絶縁パッキング4とによって形成さ
れるくぼみ部Bに充填され硬化されている。5は発電要
素の正極の活物質から導出されたリード線で、正極の端
子2の内面に電気的に接続されている。紫外線硬化型樹
脂としてはプレポリマーとしてウレタンアクリレート樹
脂が20〜40重量部,モノマーとしてアクリル樹脂が50〜
80重量部,光重合開始剤として通常用いられるベンゾフ
ェノン,ベンゾインイソブチルエーテルなどのカルボニ
ル化合物が0.5〜1.0重量部で構成される。なお紫外線硬
化型樹脂のプレポリマー,希釈剤としてのモノマー素材
の配合量を前述のような配合にしたのは電池のくぼみ部
Bに均一に作業性良く樹脂を流し込むために必要な粘度
を得るのに最適な配合であり、また通常の紫外線硬化型
樹脂の汎用的な配合比でもある。なお希釈剤のモノマー
としてのアクリル樹脂としては、分子量が100〜300程度
粘度が1〜60cps程度のものであり、具体的な物質とし
ては、2−エチルヘキシルアクリレート、2−ヒドロキ
シプロピルアクリレート、1.6−ヘキサンジアクリレー
ト、1.3−ブタンジオールジアクリレートなどである。
次にウレタンアクリレート樹脂は、−OH基をもつアクリ
レートとジイソシアネートを等モル反応させて得られる
末端−NCO基をもつアクリレートに対し、ポリエステル
ポリオールを反応させて得られるもので、分子量が1000
〜8000程度の樹脂である。次に本発明の効果について、
他のプレポリマー樹脂を用いた紫外線硬化型樹脂との比
較実験を行なった結果を表1に示す。なお実験に際して
はモノマー樹脂,重合開始剤等はすべて同一配合条件、
つまりプレポリマー樹脂20〜40重量部,モノマー樹脂50
〜80重量部,光重合開始剤0.5〜1.0重量部の範囲内とし
た。紫外線は高圧水銀灯を光源として1500〔mJ/cm2〕の
光量で30秒間照射し、樹脂を硬化させた。表−1に示す
数字は紫外線硬化型樹脂を円筒形リチウム電池の端子く
ぼみ部Bに塗布し、硬化させたものを−40℃と、85℃の
温度条件に2時間ずつ交互に交換する熱衝撃試験機に1
サイクル4時間として、10サイクル,30サイクル,100サ
イクル熱衝撃を負荷した時の樹脂の割れについて各々10
0個のサンプルについて調査比較した結果である。In the figure, 1 is an insulating member made of an ultraviolet curable resin,
This is because the terminal plate 2 also serving as the positive electrode terminal, the metal container 3 having the power generating element A built therein and also serving as the negative electrode terminal, both terminals are insulated inside the battery, and the built-in power generating element A leaks to the outside. It is filled and hardened in the recess B formed by the insulating packing 4 for preventing the above. Reference numeral 5 is a lead wire derived from the positive electrode active material of the power generation element, and is electrically connected to the inner surface of the positive electrode terminal 2. As UV curable resin, urethane acrylate resin as prepolymer is 20-40 parts by weight, acrylic resin as monomer is 50-
80 parts by weight, 0.5 to 1.0 part by weight of carbonyl compounds such as benzophenone and benzoin isobutyl ether that are commonly used as photopolymerization initiators. The prepolymer of the UV-curable resin and the monomer material as a diluent are blended in the amounts as described above in order to obtain the viscosity required for pouring the resin uniformly into the recess B of the battery with good workability. Is the most suitable compounding ratio, and is also a general-purpose compounding ratio for ordinary UV-curable resins. The acrylic resin as a monomer of the diluent has a molecular weight of about 100 to 300 and a viscosity of about 1 to 60 cps, and specific substances include 2-ethylhexyl acrylate, 2-hydroxypropyl acrylate, and 1.6-hexane. Examples thereof include diacrylate and 1.3-butanediol diacrylate.
Next, the urethane acrylate resin is obtained by reacting a polyester polyol with an acrylate having a terminal -NCO group obtained by reacting an acrylate having a -OH group with a diisocyanate in an equimolar manner, and has a molecular weight of 1,000.
It is about 8000 resin. Next, regarding the effect of the present invention,
Table 1 shows the results of a comparison experiment with an ultraviolet curable resin using another prepolymer resin. In addition, in the experiment, the monomer resin, the polymerization initiator, etc. all had the same compounding conditions,
That is, 20-40 parts by weight of prepolymer resin and 50 parts of monomer resin
-80 parts by weight and 0.5 to 1.0 part by weight of the photopolymerization initiator. Ultraviolet rays were irradiated for 30 seconds with a light amount of 1500 [mJ / cm 2 ] using a high pressure mercury lamp as a light source to cure the resin. The numbers shown in Table-1 are thermal shocks in which UV curable resin is applied to the terminal recess B of a cylindrical lithium battery and the cured product is alternately exchanged for 2 hours under the temperature conditions of -40 ° C and 85 ° C. 1 for testing machine
A cycle of 4 hours, 10 cycles, 30 cycles, 100 cycles, 10 cycles each for resin cracking when thermal shock was applied
It is the result of the investigation and comparison of 0 samples.
発明の効果 以上、表−1の実験結果から明らかなように本発明のウ
レタンアクリレート樹脂をプレポリマーとして配合した
紫外線硬化型樹脂は、熱衝撃等の環境ストレスに対し極
めて有効なものであり、長期信頼性に優れる電池を提供
するものである。 Effects of the Invention As is clear from the experimental results in Table 1 above, the ultraviolet-curable resin containing the urethane acrylate resin of the present invention as a prepolymer is extremely effective against environmental stress such as thermal shock, It is intended to provide a battery with excellent reliability.
第1図は本発明の紫外線硬化型樹脂を絶縁性部材として
用いた電池の要部断面図である。 1……紫外線硬化型樹脂、2,3……正・負極端子、4…
…絶縁パッキング、A……発電要素、B……くぼみ。FIG. 1 is a sectional view of a main part of a battery using the ultraviolet curable resin of the present invention as an insulating member. 1 ... UV curable resin, 2, 3 ... Positive / negative electrode terminals, 4 ...
… Insulating packing, A… Power generation element, B… Dimple.
Claims (2)
の間に形成されたくぼみ部分に、紫外線硬化型の樹脂を
絶縁部材として充填した電池であって、紫外線硬化型樹
脂の光重合性プレポリマーがウレタンアクリレート樹
脂,光重合性モノマーがアクリル樹脂からなることを特
徴とする電池。1. A battery in which a recessed portion formed between a positive electrode terminal and a negative electrode terminal exposed on the same surface is filled with an ultraviolet curable resin as an insulating member, which is a photopolymerizable prepolymer of the ultraviolet curable resin. A battery in which the polymer is a urethane acrylate resin and the photopolymerizable monomer is an acrylic resin.
プレポリマーが20〜40重量部,光重合性モノマーが50〜
80重量部である特許請求の範囲第1項記載の電池。2. The ultraviolet curable resin is compounded in an amount of 20 to 40 parts by weight of a photopolymerizable prepolymer and 50 to 50 parts of a photopolymerizable monomer.
The battery according to claim 1, which is 80 parts by weight.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1058310A JPH0793131B2 (en) | 1989-03-10 | 1989-03-10 | Battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1058310A JPH0793131B2 (en) | 1989-03-10 | 1989-03-10 | Battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02236950A JPH02236950A (en) | 1990-09-19 |
JPH0793131B2 true JPH0793131B2 (en) | 1995-10-09 |
Family
ID=13080670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1058310A Expired - Fee Related JPH0793131B2 (en) | 1989-03-10 | 1989-03-10 | Battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0793131B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005011545A (en) * | 2003-06-16 | 2005-01-13 | Nec Tokin Tochigi Ltd | Sealed battery |
JP5371451B2 (en) * | 2009-01-08 | 2013-12-18 | 日立マクセル株式会社 | Battery and manufacturing method thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS56159055A (en) * | 1980-05-13 | 1981-12-08 | Yuasa Battery Co Ltd | Battery |
JPS60163911A (en) * | 1984-02-02 | 1985-08-26 | Suriibondo:Kk | Photocurable rubbery elastic composition |
-
1989
- 1989-03-10 JP JP1058310A patent/JPH0793131B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH02236950A (en) | 1990-09-19 |
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Legal Events
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FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20081009 Year of fee payment: 13 |
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