JPH02236950A - Cell - Google Patents

Cell

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Publication number
JPH02236950A
JPH02236950A JP1058310A JP5831089A JPH02236950A JP H02236950 A JPH02236950 A JP H02236950A JP 1058310 A JP1058310 A JP 1058310A JP 5831089 A JP5831089 A JP 5831089A JP H02236950 A JPH02236950 A JP H02236950A
Authority
JP
Japan
Prior art keywords
resin
photopolymerizing
battery
prepolymer
terminal
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.)
Granted
Application number
JP1058310A
Other languages
Japanese (ja)
Other versions
JPH0793131B2 (en
Inventor
Fumio Oo
大尾 文夫
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP1058310A priority Critical patent/JPH0793131B2/en
Publication of JPH02236950A publication Critical patent/JPH02236950A/en
Publication of JPH0793131B2 publication Critical patent/JPH0793131B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries

Landscapes

  • Sealing Battery Cases Or Jackets (AREA)

Abstract

PURPOSE:To improve crack resistance by filling the dent portion between positive and negative electrodes exposed to the same plane with ultraviolet curing resin whose photopolymerizing prepolymer and photopolymerizing monomer are specified respectively. CONSTITUTION:An insulating member 1 consisting of ultraviolet curing resin is cured after a dent portion B formed of a terminal assembly 2 which doubles as a positive electrode terminal, a metal case 3 which contains a generating element A and doubles as the terminal of a negative electrode and an insulating packing 4 is filled with the insulating member 1. Photopolymerizing prepolymer used for ultraviolet curing resin 1 consists of urethane acrylate resin and photopolymerizing monomer used therefore consists of acryl resin. Thus, it is possible to reduce an internal strain after curing and also improve crack resistance.

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。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a battery constructed by filling an exposed terminal surface of the battery with an ultraviolet curing 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、内蔵電解液が月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、従来よシ金属との密着性.接
着性に浸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シ、
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。
Conventional technology Conventionally, an insulating material is interposed between the positive and negative terminals of a battery that are exposed on the same surface to prevent short circuits caused by contact with external metal parts or liquid leaks caused by condensation. Efforts were made to prevent the phenomenon. Especially in the case of high-output batteries such as lithium batteries or alkaline batteries, when a short circuit occurs, a large current will flow, the battery itself will generate heat, the battery seal may become deformed, and the built-in electrolyte may damage the device in which it is used. When water or other liquid is present between the two electrode terminals and a liquid junction occurs, electrolysis of water occurs in batteries with a potential of 3V, such as lithium batteries, which corrodes the metal terminals. There were other problems. Insulating materials that solve these problems are those that have better adhesion to metals than conventional ones. Polymeric materials have been used that provide adhesive properties. These adhesives are mainly solvent-soluble or two-component adhesive compositions, but they require a long time to harden.
Solvent-soluble types require a step to scatter the solvent in the production line, which increases battery manufacturing costs. On the other hand, UV-curable adhesive compositions are solvent-free and consist of a photopolymerizable prepolymer with a reactive group such as a double bond in the molecule, a photopolymerizable monomer as a diluent, and a photoreaction initiator as the main components. It is a mold adhesive composition that instantly cures the adhesive by irradiating it with ultraviolet light, so it is becoming widely used.

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o.3″g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大意的な環境ストレヌに
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。
Problems to be Solved by the Invention As described above, the adhesive curing reaction of an ultraviolet curable resin is caused by a polymerization reaction between a photopolymerizable prepolymer and a photopolymerizable monomer when irradiated with ultraviolet rays, resulting in adhesive curing. For this reason, if the resin is thick, specifically o. When the wall thickness is 3"g or more, the photopolymerization reaction starts from the surface layer of the resin, so the curing rate of the resin is different between the surface layer and the inner layer. Since the degree of polymerization is different, the hardening rate of the resin after curing is Adhesive curing reaction takes place in a state where strain is contained inside the resin.In this way, when the resin adheres and hardens on the exposed surface of the terminal as an insulating member with the strain remaining inside the resin, it will cause damage during battery storage and use. Cracks often occur on the resin surface due to long-term environmental stress caused by the natural environment or significant environmental stress such as short-term thermal shock, rendering it useless 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4@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ノレ樹脂が60〜80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K介在させたものである。
Means for Solving the Problems The present invention has solved the above-mentioned problems by conducting intensive studies on 4@materials and using 20 to 40 parts by weight of urethane acrylate resin as a photopolymerizable prepolymer. By using an ultraviolet curable resin containing 60 to 80 parts by weight of acrinole resin as a photopolymerizable monomer, the internal strain after curing is small, and an insulating member with excellent crack resistance is interposed in the exposed terminal part K of the battery. be.

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。
Effect: Compared to other general-purpose UV-curable resins, the UV-curable resin with the above-mentioned formulation forms a polyurethane structure and produces a relatively viscous and elastic cured product. It is thought that this has the effect 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
Embodiment FIG. 1 is a sectional view of a main part of a battery showing an embodiment 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、発電要素人を内
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人が外部に漏
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
素の正樺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T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
60〜sofi量部.光重合開始剤として通常用いられ
るペンゾフェノン.ペンゾインイソプチノレエーテルな
どのカルボニル化合物が0.6〜1.0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)V樹脂としては、
分−I−量が100〜300程度粘度が1〜eocpS
程度のものであり、具体的な物質としては、2−エチル
へキシルアクリレート、2−ヒドロキグロビルアクリレ
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
クリレート樹脂ハ、−OH基をもつアクリレートとジイ
ソシアネートを等七ル反応させて得られる未端−HOO
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1000〜80
00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詣20〜40重量部.モノマー樹脂
60〜80重量部,光重合開始剤Q5〜1.0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160
0〔I!IJ/cI〕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’Cと、86℃の温度条件に2時間ずつ
交互に変換する熱衝撃試験機に1サイク/L’4時間と
して、1o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100個の
サンプルについて調査比較した結果である。
1 in the figure is an insulating member made of ultraviolet curable resin,
This consists of a terminal board 2 that also serves as the positive terminal, a metal container 3 that houses the power generating element and also serves as the negative terminal, and insulation between both terminals inside the battery, as well as to prevent the built-in power generating element from leaking outside. The concave portion B formed by the insulating packing 4 to prevent this is filled and hardened. Reference numeral 5 denotes a lead wire derived from the active material of Japanese birch of the power generation element, and is electrically connected to the inner surface of the positive electrode terminal 2. The ultraviolet curable resin includes 20 to 40 parts by weight of urethane acrylate resin as a prepolymer and 60 to SOFI parts of acrylic resin as a monomer. Penzophenone is commonly used as a photopolymerization initiator. A carbonyl compound such as penzoin isoptynolether is comprised in an amount of 0.6 to 1.0 parts by weight. Note that this is a prepolymer of UV-curable resin. The blending amount of the monomer material as a diluent as described above is the optimum blend to obtain the viscosity necessary to pour the resin uniformly into the recess B of the battery with good workability, and it is also It is also a general-purpose blending ratio for ultraviolet curable resins. In addition, as the acrylic) V resin as the diluent monomer,
Min-I amount is about 100-300 viscosity is 1-eocpS
Specific substances include 2-ethylhexyl acrylate, 2-hydroxyglovir acrylate, 1,6-hexane diacrylate, and 1,3-butanediol diacrylate. Next, the urethane acrylate resin is an unterminated -HOO obtained by reacting an acrylate with an -OH group with a diisocyanate.
It is obtained by reacting a polyester polyol with an acrylate having a group, and has a molecular weight of 1000 to 80.
It is a resin of about 0.00. Next, regarding the effects of the present invention, Table 1 shows the results of a comparative experiment with ultraviolet curable resins using other prepolymer resins. In addition, monomer resin was used in the experiment. All polymerization initiators were mixed under the same conditions, that is, 20 to 40 parts by weight of the prepolymer. The monomer resin was in the range of 60 to 80 parts by weight, and the photopolymerization initiator Q was in the range of 5 to 1.0 parts by weight. Ultraviolet light is 160% using a high-pressure mercury lamp as a light source.
0 [I! IJ/cI] for 30 seconds to cure the resin. The numbers shown in Table 1 are the heat applied to the terminal recess B of a cylindrical lithium battery with ultraviolet curable resin and the cured resin heated to -40'C and 86°C alternately for 2 hours. The impact tester was subjected to 1o cycles at 1 cycle/L'4 hours. These are the results of an investigation and comparison of 100 samples each regarding cracking of the resin when thermal shock was applied for 30 cycles and 100 cycles.

(以 下 余白) 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。
(Left below) Effects of the invention As is clear from the experimental results in Table 1, 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. This provides a battery with excellent long-term reliability.

【図面の簡単な説明】[Brief explanation of drawings]

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、▲・・
・・・・発電要素、B・・・・・・くぼみ。 代理人の氏名 弁理士 粟 野 重 孝 ほか1名t−
1卜玖石更化クg,尉龍 2−LPI!%÷ A−一一発臂蓼索
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... Ultraviolet curing resin, 2.3...
Positive/negative terminals, 4... Insulation packing, ▲...
...Power generation element, B...Indentation. Name of agent: Patent attorney Shigetaka Awano and one other person
1 卜玖石sarakakug, Yoryu 2-LPI! % ÷ A - 11 strokes

Claims (2)

【特許請求の範囲】[Claims] (1)同一面に露出する正極端子および負極端子の間に
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 recess 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, and the photopolymerizable prepolymer of the ultraviolet curable resin is A battery characterized in that a urethane acrylate resin and a photopolymerizable monomer are made of an acrylic resin.
(2)紫外線硬化型樹脂の配合量として光重合性プレポ
リマーが20〜40重量部、光重合性モノマーが60〜
80重量部である特許請求の範囲第1項記載の電池。
(2) The amount of UV curable resin is 20 to 40 parts by weight of photopolymerizable prepolymer and 60 to 60 parts by weight of photopolymerizable monomer.
80 parts by weight of the battery according to claim 1.
JP1058310A 1989-03-10 1989-03-10 Battery Expired - Fee Related JPH0793131B2 (en)

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 true JPH02236950A (en) 1990-09-19
JPH0793131B2 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)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005011545A (en) * 2003-06-16 2005-01-13 Nec Tokin Tochigi Ltd Sealed battery
JP2010160977A (en) * 2009-01-08 2010-07-22 Hitachi Maxell Ltd Battery and its manufacturing method

Citations (2)

* Cited by examiner, † Cited by third party
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

Patent Citations (2)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005011545A (en) * 2003-06-16 2005-01-13 Nec Tokin Tochigi Ltd Sealed battery
JP2010160977A (en) * 2009-01-08 2010-07-22 Hitachi Maxell Ltd Battery and its manufacturing method

Also Published As

Publication number Publication date
JPH0793131B2 (en) 1995-10-09

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