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JPS624826B2 - - Google Patents
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JPS624826B2 - - Google Patents

Info

Publication number
JPS624826B2
JPS624826B2 JP6746277A JP6746277A JPS624826B2 JP S624826 B2 JPS624826 B2 JP S624826B2 JP 6746277 A JP6746277 A JP 6746277A JP 6746277 A JP6746277 A JP 6746277A JP S624826 B2 JPS624826 B2 JP S624826B2
Authority
JP
Japan
Prior art keywords
molecular weight
sealant
polyfluoroalkoxyphosphazene
alkaline
sealing plate
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
Application number
JP6746277A
Other languages
Japanese (ja)
Other versions
JPS541831A (en
Inventor
Kenichi Yokoyama
Akira Kawakami
Noboru Kotani
Motoko Yoshida
Tetsuichi Kudo
Hidehito Oohayashi
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.)
Hitachi Ltd
Maxell Ltd
Original Assignee
Hitachi Ltd
Hitachi Maxell 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 Hitachi Ltd, Hitachi Maxell Ltd filed Critical Hitachi Ltd
Priority to JP6746277A priority Critical patent/JPS541831A/en
Publication of JPS541831A publication Critical patent/JPS541831A/en
Publication of JPS624826B2 publication Critical patent/JPS624826B2/ja
Granted legal-status Critical Current

Links

Classifications

    • Y02E60/12

Landscapes

  • Sealing Battery Cases Or Jackets (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は銀電池、水銀電池、ニツケルカドミウ
ム電池、アルカリマンガン電池などのアルカリ電
池における封口部の改良に係り、耐漏液性の向上
を計ることを目的とする。 従来この種の電池において、ガスケツトと封口
板の間、をアスフアルトピツチ、脂肪ポリアミド
樹脂、低重合度のフツ素樹脂、ポリイソブチレン
などのシール剤で充塞して、前述の接面からの漏
液を防止することが提案されている。ところが前
述のようなシール剤では、加圧下でアルカリ電解
液と長期間接触していたり、あるいは低温から高
温までの熱履歴を繰り返すことにより変質が起こ
り、シール剤の弾力性や撥水性が低下して、シー
ル剤を介在した効果が十分に発揮されず漏液を生
じていた。 本発明はガスケツトと封口板の間を、高分子量
ポリフルオロアルコキシホスフアゼンと低分子量
ポリフルオロアルコキシホスフアゼンの混合物か
らなるシール剤で充塞することにより、長期間安
定した液密効果を有するアルカリ電池を提供する
ものである。 ホスフアゼンとは、窒素とリンの結合を骨格と
して、これらが交互に配列された化合物で、五塩
化リンをテトラクロロエタン、クロルベンゾー
ル、ニトロベンゾールなどの有機溶剤に溶かし、
これと塩化アンモニウムを反応することによつて
得られる結晶体で(PNCl2nで表わされ(但しm
は3あるいは4の整数)、mが3の場合は下記(1)
に示すような環状構造を有している。 これは加熱により容易に開環重合して、下記(2)
に示すような高分子化合物となりゴム弾性を有し
ているが、式中のリンと塩素の結合は極めて不安
定で、空気中の水分を吸湿して加水分解するた
め、アルカリ電池のシール剤としては不適当であ
る。 そのため本発明では前記高分子化合物(2)に例え
ばCF3ONa、CF3CH2ONa、HC2F4CH2ONa、
HC3F6CH2ONa、C6H4FOK、C6H4CF3OKなどの
フルオロアルコキシドの1種もしくは2種以上を
反応して得られたポリフルオロアルコキシホスフ
アゼンをシール剤として使用したもので、それら
の構造式を例示すれば次の通りであり、側鎖にフ
ツ化炭化水素を有するホスフアゼンポリマーの一
種である。 このポリフルオロアルコキシホスフアゼンは、
例えば前記構造式(1)で示されるホスフアゼンを硝
子管中に導入し、これを真空に引いた上で密封
し、加熱重合反応させて前記高分子化合物(2)にフ
ルオロアルコキシドの一種もしくは二種以上を反
応させ、前記高分子化合物(2)のCl基とフルオロ
アルコキシド基を置換することにより得られる。 ポリフルオロアルコキシホスフアゼンの分子量
はホスフアゼンを加熱重合反応をさせて高分子化
合物(2)をつくる際の重合温度により調整でき、分
子量が約3×104ないし3×106程度の高分子量の
ものは重合温度を約230℃〜280℃程度、分子量が
約4×103程度までの低分子量のものは約200℃〜
220℃の温度で得られる。 このように製造条件によつて、分子量が約3×
104ないし3×106程度の高分子量のものから、分
子量が約4×103程度までの低分子量のものまで
種々得られる。ポリフルオロアルコキシホスフア
ゼンの高分子量のものは、低温から高温までの熱
履歴を繰り返しても撥水性の低下がなく、しかも
加圧下で高濃度のアルカリ溶液中に長期間浸漬し
ても全く変質がなく化学的に極めて安定している
が、柔軟性ならびに伸びが十分でない。一方ポリ
フルオロアルコキシホスフアゼンの低分子量のも
のは、高い弾性率と伸びを示し、ガスケツトおよ
び封口板の表面に形成されている微細な凹凸によ
く密着するが、前記高分子量ポリフルオロアルコ
キシホスフアゼンに比べ、低温から高温までの熱
履歴を繰り返した場合若干の撥水性の低下が生
じ、しかも加圧下で高濃度のアルカリ溶液中に長
期間浸漬した場合若干の変質が生じるという欠点
を有する。したがつて高分子量のポリフルオロア
ルコキシホスフアゼンと低分子量のポリフルオロ
アルコキシホスフアゼンを混合したものをシール
剤として使用することにより、それぞれの欠点を
相補い、両者の優れた性質を選択的に発揮するこ
とができる。なお本発明によるポリフルオロアル
コキシホスフアゼンの溶剤には、例えばケトン
類、エステル類、テトロヒドロフランなどの有機
液体が用いられる。 次に本発明の実施例について第1図を用いて説
明する。 酸化銀や酸化水銀などの陽極活物質と、リン状
黒鉛やアセチレンブラツクなどの電導剤との混合
粉末を加圧成形し、周辺部に断面L字状の金属製
台座1を一体に装着した円板状の陽極2を、ニツ
ケルメツキした鉄缶からなり陽極端子を兼ねた電
池容器3の缶底に挿入する。電池容器3の缶底に
は予め所定量のアルカリ電解液が注入されてお
り、陽極2の挿入により電解液は陽極2の細孔に
浸透して陽極全体を湿潤する。陽極2の上にはポ
リオレフインの微孔性フイルムにアクリル酸やメ
タクリル酸をグラフト重合した阻止膜4、セロフ
アンやポリビニルアルコールフイルムなどからな
る半透膜5、ポリプロピレン繊維の不織布やビニ
ロン繊維とビスコースレイヨン繊維の混抄紙など
からなる吸液紙6が順次載置されている。 陰極端子を兼ねた封口板7の周辺部には断面が
U字状もしくはV字状の垂下部8が形成されてお
り、この垂下部8の内側から外側の端縁エツジに
かけて、分子量が約3×104ないし3×106の高分
子量ポリフルオロアルコキシホスフアゼンと、分
子量が約4×103までの低分子量ポリフルオロア
ルコキシホスフアゼンの混合物を有機溶剤に溶解
した液体を塗布し乾燥して、連続したシール剤の
被膜9が形成されている。垂下部8の外側にはポ
リエチレン、ポリプロピレン、ポリアミドなどの
合成樹脂からなり断面L字状のガスケツト10が
嵌合されており、封口板7の内側にはアマルガム
化した亜鉛粉末と、ポリアクリル酸塩などのゲル
化剤でゲル状になつたアルカリ電解液の混合物か
らなる陰極剤11が充填されている。 この封口板7ならびにガスケツト10を電池容
器3の開口端12に嵌合し、該開口端12を内方
へ絞りガスケツト10を圧縮させて高い接面圧を
発揮させるとともに、電池容器3の開口端12と
対向するように上方へ向いた封口板7の端縁エツ
ジ13を、シール剤の被膜9を介してガスケツト
10に食い込ませてボタン型アルカリ電池を組立
てる。 第1図に示す本発明のアルカリ電池、ならびに
従来のシール剤を用いた同型のアルカリ電池を35
℃、相対湿度80%で保存した際の漏液発生率を次
の表に示す。なお表に示されるものは、第1図図
示の構造の電池に適用したものであり、ガスケツ
トと封口板の間をシール剤で充塞したものであ
る。
The present invention relates to an improvement in the sealing part of alkaline batteries such as silver batteries, mercury batteries, nickel cadmium batteries, alkaline manganese batteries, etc., and an object of the present invention is to improve leakage resistance. Conventionally, in this type of battery, the space between the gasket and the sealing plate is filled with a sealant such as asphalt pitch, fatty polyamide resin, low polymerization degree fluororesin, or polyisobutylene to prevent liquid from leaking from the contact surfaces mentioned above. It is proposed that. However, with the sealant mentioned above, deterioration occurs due to long-term contact with alkaline electrolyte under pressure or repeated thermal history from low to high temperatures, resulting in a decrease in the elasticity and water repellency of the sealant. Therefore, the effect of using a sealant was not sufficiently exerted, resulting in leakage. The present invention provides an alkaline battery that has a stable liquid-tight effect over a long period of time by filling the space between the gasket and the sealing plate with a sealant made of a mixture of high molecular weight polyfluoroalkoxyphosphazene and low molecular weight polyfluoroalkoxyphosphazene. It is something. Phosphazene is a compound in which nitrogen and phosphorus bonds are arranged alternately as a backbone. Phosphazene is a compound in which phosphorus pentachloride is dissolved in an organic solvent such as tetrachloroethane, chlorobenzole, or nitrobenzole.
A crystalline substance obtained by reacting this with ammonium chloride, represented by (PNCl 2 ) n (where m
is an integer of 3 or 4), if m is 3, use the following (1)
It has a cyclic structure as shown in . This easily undergoes ring-opening polymerization by heating, resulting in the following (2)
It is a polymer compound as shown in the formula and has rubber elasticity, but the bond between phosphorus and chlorine in the formula is extremely unstable, and because it absorbs moisture in the air and hydrolyzes it, it is used as a sealant for alkaline batteries. is inappropriate. Therefore, in the present invention, the polymer compound (2) includes, for example, CF 3 ONa, CF 3 CH 2 ONa, HC 2 F 4 CH 2 ONa,
A polyfluoroalkoxyphosphazene obtained by reacting one or more fluoroalkoxides such as HC 3 F 6 CH 2 ONa, C 6 H 4 FOK, and C 6 H 4 CF 3 OK was used as a sealant. Examples of their structural formulas are as follows, and they are a type of phosphazene polymer having a fluorinated hydrocarbon in the side chain. This polyfluoroalkoxyphosphazene is
For example, the phosphazene represented by the structural formula (1) is introduced into a glass tube, the tube is evacuated and sealed, and the polymer compound (2) is converted into one or two fluoroalkoxides by heating and polymerizing the tube. It is obtained by reacting the above and substituting the Cl group and fluoroalkoxide group of the polymer compound (2). The molecular weight of polyfluoroalkoxyphosphazene can be adjusted by the polymerization temperature at which the polymer compound (2) is produced by subjecting phosphazene to a heating polymerization reaction, and polyfluoroalkoxyphosphazene has a high molecular weight of about 3 x 10 4 to 3 x 10 6 . The polymerization temperature is about 230°C to 280°C, and the polymerization temperature is about 200°C to about 200°C for low molecular weight ones with a molecular weight of up to about 4 x 103 .
Obtained at a temperature of 220°C. In this way, depending on the manufacturing conditions, the molecular weight is approximately 3×
A variety of compounds can be obtained, ranging from those with a high molecular weight of about 10 4 to 3×10 6 to those with a low molecular weight of about 4×10 3 . High-molecular-weight polyfluoroalkoxyphosphazenes do not lose their water repellency even after repeated thermal cycles from low to high temperatures, and they do not deteriorate at all even when immersed in high-concentration alkaline solutions under pressure for long periods of time. Although it is chemically extremely stable, it does not have sufficient flexibility or elongation. On the other hand, low molecular weight polyfluoroalkoxyphosphazenes exhibit high elastic modulus and elongation, and adhere well to minute irregularities formed on the surfaces of gaskets and sealing plates. In comparison, it has the disadvantage that water repellency slightly decreases when the thermal history is repeated from low to high temperatures, and furthermore, when immersed in a high concentration alkaline solution under pressure for a long period of time, some deterioration occurs. Therefore, by using a mixture of high molecular weight polyfluoroalkoxyphosphazene and low molecular weight polyfluoroalkoxyphosphazene as a sealant, the drawbacks of each can be compensated for and the excellent properties of both can be selectively exhibited. can do. Note that organic liquids such as ketones, esters, and tetrahydrofuran are used as the solvent for the polyfluoroalkoxyphosphazene according to the present invention. Next, an embodiment of the present invention will be described with reference to FIG. A circle is formed by pressure molding a mixed powder of anode active material such as silver oxide or mercury oxide and a conductive agent such as phosphorous graphite or acetylene black, and a metal pedestal 1 having an L-shaped cross section is integrally attached to the periphery. A plate-shaped anode 2 is inserted into the bottom of a battery container 3, which is made of a nickel-plated iron can and also serves as an anode terminal. A predetermined amount of alkaline electrolyte is injected into the bottom of the battery container 3 in advance, and when the anode 2 is inserted, the electrolyte permeates into the pores of the anode 2 and wets the entire anode. On the anode 2 are a blocking membrane 4 made of a microporous polyolefin film graft-polymerized with acrylic acid or methacrylic acid, a semipermeable membrane 5 made of cellophane or polyvinyl alcohol film, and a nonwoven fabric of polypropylene fiber, vinylon fiber, and viscose rayon. Absorbent papers 6 made of fiber-mixed paper or the like are placed one after another. A hanging part 8 having a U-shaped or V-shaped cross section is formed at the periphery of the sealing plate 7 which also serves as a cathode terminal. A mixture of a high molecular weight polyfluoroalkoxyphosphazene having a molecular weight of ×10 4 to 3 × 10 6 and a low molecular weight polyfluoroalkoxyphosphazene having a molecular weight of up to about 4 × 10 3 dissolved in an organic solvent is applied and dried. A continuous sealant coating 9 is formed. A gasket 10 made of synthetic resin such as polyethylene, polypropylene, polyamide, etc. and having an L-shaped cross section is fitted on the outside of the hanging part 8, and amalgamated zinc powder and polyacrylic acid salt are fitted on the inside of the sealing plate 7. The cathode material 11 is filled with a mixture of an alkaline electrolyte gelled with a gelling agent such as the following. The sealing plate 7 and gasket 10 are fitted into the open end 12 of the battery container 3, and the open end 12 is squeezed inward to compress the gasket 10 and exert a high contact pressure. The edge edge 13 of the sealing plate 7 facing upward so as to face the sealing plate 12 is bitten into the gasket 10 through the sealant coating 9 to assemble the button-type alkaline battery. The alkaline battery of the present invention shown in Figure 1 and the same type of alkaline battery using a conventional sealant were tested at 35
The following table shows the leakage rate when stored at ℃ and 80% relative humidity. The battery shown in the table was applied to a battery having the structure shown in FIG. 1, in which the space between the gasket and the sealing plate was filled with a sealant.

【表】【table】

【表】 この表から明らかなように、本発明によるアル
カリ電池は優れた耐漏液性を有している。 低分子量ポリフルオロアルコキシホスフアゼン
の好適な混合比率は約5〜60重量%で、さらに好
ましくは約10〜30重量%である。 また混合シール剤に代え複合膜シール剤を使用
することも考えられるが複合膜をつくるには、少
くとも2回の膜形成工程が必要であり、作業が煩
雑になり好ましくない。
[Table] As is clear from this table, the alkaline battery according to the present invention has excellent leakage resistance. A preferred mixing ratio of low molecular weight polyfluoroalkoxyphosphazenes is about 5-60% by weight, more preferably about 10-30% by weight. It is also conceivable to use a composite membrane sealant instead of the mixed sealant, but this is not preferable since it requires at least two membrane formation steps to form a composite membrane, making the work complicated.

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

第1図は本発明の実施例によるボタン型アルカ
リ電池の全体断面図である。 3…電池容器、7…封口板、9…シール剤、1
0…ガスケツト。
FIG. 1 is an overall sectional view of a button-type alkaline battery according to an embodiment of the present invention. 3...Battery container, 7...Sealing plate, 9...Sealant, 1
0...Gasket.

Claims (1)

【特許請求の範囲】[Claims] 1 ガスケツトと封口板の間を、高分子量ポリフ
ルオロアルコキシホスフアゼンと低分子量ポリフ
ルオロアルコキシホスフアゼンの混合物からなる
シール剤で充塞したことを特徴とするアルカリ電
池。
1. An alkaline battery characterized in that the space between the gasket and the sealing plate is filled with a sealant made of a mixture of high molecular weight polyfluoroalkoxyphosphazene and low molecular weight polyfluoroalkoxyphosphazene.
JP6746277A 1977-06-07 1977-06-07 Alkaline cell Granted JPS541831A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6746277A JPS541831A (en) 1977-06-07 1977-06-07 Alkaline cell

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6746277A JPS541831A (en) 1977-06-07 1977-06-07 Alkaline cell

Publications (2)

Publication Number Publication Date
JPS541831A JPS541831A (en) 1979-01-09
JPS624826B2 true JPS624826B2 (en) 1987-02-02

Family

ID=13345632

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6746277A Granted JPS541831A (en) 1977-06-07 1977-06-07 Alkaline cell

Country Status (1)

Country Link
JP (1) JPS541831A (en)

Also Published As

Publication number Publication date
JPS541831A (en) 1979-01-09

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