JPS6411074B2 - - Google Patents
Info
- Publication number
- JPS6411074B2 JPS6411074B2 JP2892383A JP2892383A JPS6411074B2 JP S6411074 B2 JPS6411074 B2 JP S6411074B2 JP 2892383 A JP2892383 A JP 2892383A JP 2892383 A JP2892383 A JP 2892383A JP S6411074 B2 JPS6411074 B2 JP S6411074B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- paint
- coating film
- coating
- inorganic
- 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
Links
- 239000003973 paint Substances 0.000 claims description 26
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 24
- 239000008119 colloidal silica Substances 0.000 claims description 8
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 5
- 239000007822 coupling agent Substances 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 3
- 239000000945 filler Substances 0.000 claims 1
- 239000011248 coating agent Substances 0.000 description 26
- 238000000576 coating method Methods 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 239000011256 inorganic filler Substances 0.000 description 6
- 229910003475 inorganic filler Inorganic materials 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- 239000001023 inorganic pigment Substances 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 230000009965 odorless effect Effects 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 150000003609 titanium compounds Chemical class 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 230000002159 abnormal effect Effects 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003985 ceramic capacitor Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Details Of Resistors (AREA)
- Coils Or Transformers For Communication (AREA)
Description
産業上の利用分野
本発明は、過負荷や自己発熱を伴う電子部品,
すなわち抵抗器,フイルムコンデンサ,セラミツ
クコンデンサ,コイル,各種ヒータ等の被覆材と
して使用される電子部品用不燃性塗料に関するも
のである。
従来例の構成とその問題点
一般の電子部品用塗料は有機系を主とし、エポ
キシ系,フエノール系及び難燃性に優れるシリコ
ン系が知られ、実用化されている。しかし、いず
れも塗料の硬化焼付時間が長く(30分〜2時間)
また難燃性に優れたシリコン系は高温(180℃以
上)にて焼付しなければならず、電子部品の製作
工程上で量産性に欠け、かつ省エネルギーの観点
からも不向きとされているものの多用されている
のが現状である。特に最近では、電子部品製作工
程上の安全性の意味から、無臭,無煙で、かつ引
火爆発性のない無機質からなる不燃性塗料の開発
が切望されているのが現状である。
発明の目的
本発明は上記のような点に鑑みなされたもので
あり、低温(約160℃)かつ短時間(約10分)の
焼付硬化を可能とし、また引火性がなく保安上安
全で、無臭性を有すると共に過負荷に伴う自己発
熱や外部からの発炎に対しても着火することな
く、しかも耐湿性等の品質特性も従来品と同等か
それ以上の性能を有し、異常な過負荷や自己発熱
を伴う電子部品用被覆材として好適な電子部品用
不燃性塗料を提供することを目的とするものであ
る。
発明の構成
この目的を達成するために本発明の電子部品用
不燃性塗料は、シリカ固形成分1%〜40%を有す
る水性コロイダルシリカ1部〜30部とエチルシリ
ケート単量体1部〜5部をチタネート系カツプリ
ング剤1部〜2部を触媒として加水分解させたも
のをバインダー成分として、それにシリカ粉、ア
ルミナ粉、マイカ切片等の無機質フイラー50部〜
70部、及び必要に応じて無機顔料を混合して均一
な液状スラリーとして塗料化したものである。
この構成によれば、上記バインダー成分におい
て、加水分解生成物中のシラノールとチタン化合
物は容易に結合し架橋密度が大きく、薄い均一な
皮膜を形成する。特に、チタン化合物の無機質と
結合する部分とシラノールによるエテルシリケー
トに親和する部分とが相乗的に架橋するものと思
われる。従つて、本塗料の被覆されるべき電子部
品の素体を構成する金属面やガラス質の表面に対
し、機械的な密着性が良好である。このようなバ
インダー成分に無機質フイラーと必要に応じて無
機顔料を混合してなる塗料は、焼付温度150℃〜
170℃,焼付時間10分〜15分の硬化処理により脱
水縮合し、有害ガスの発生もなく、セラミツク状
のシロキサンとなり、緻密な塗膜を形成する。
実施例の説明
以下、本発明の実施例について説明する。ま
ず、下記の表1に示すようにチタネート系カツプ
リング剤1部,2部を触媒として水性コロイダル
シリカ(シリカ固形成分20%)25部とエチルシリ
ケート単量体5部を加水分解させたものをバイン
ダー成分として、それに無機質フイラー70部及び
無機顔料1部を混合して均一な液状スラリーとし
て塗料化した。また、チタネート系カツプリング
剤を0部とし、他は上記配合比と同一とした場合
を比較例として表1に併せて示している。この時
の塗料としての塗膜特性を下記の表2に示す。
Industrial Application Field The present invention is applicable to electronic components that are overloaded or self-heating,
In other words, it relates to nonflammable paints for electronic parts used as coating materials for resistors, film capacitors, ceramic capacitors, coils, various heaters, etc. Construction of conventional examples and their problems Common paints for electronic parts are mainly organic, and epoxy-based, phenol-based, and silicon-based paints with excellent flame retardancy are known and put into practical use. However, in both cases, the curing and baking time of the paint is long (30 minutes to 2 hours).
In addition, silicon-based materials with excellent flame retardancy must be baked at high temperatures (over 180°C), and are not suitable for mass production in the manufacturing process of electronic components, and are considered unsuitable from an energy-saving perspective, but are often used. The current situation is that Particularly in recent years, from the standpoint of safety in the manufacturing process of electronic components, there has been a strong desire to develop nonflammable paints made of inorganic materials that are odorless, smokeless, and non-flammable and explosive. Purpose of the Invention The present invention has been made in view of the above points, and enables baking hardening at low temperatures (approximately 160°C) and in a short time (approximately 10 minutes), is non-flammable, is safe from a security standpoint, It is odorless and does not ignite due to self-heating due to overload or external flames, and has quality characteristics such as moisture resistance that are equal to or better than conventional products, and does not cause abnormal overload. The object of the present invention is to provide a nonflammable paint for electronic parts that is suitable as a coating material for electronic parts that are subject to load or self-heating. Structure of the Invention To achieve this object, the nonflammable paint for electronic components of the present invention comprises 1 part to 30 parts of aqueous colloidal silica having a silica solid content of 1% to 40% and 1 part to 5 parts of ethyl silicate monomer. is hydrolyzed using 1 to 2 parts of a titanate coupling agent as a catalyst and used as a binder component, and 50 parts to 50 parts of an inorganic filler such as silica powder, alumina powder, mica chips, etc.
70 parts and an inorganic pigment as necessary are mixed to form a uniform liquid slurry into a paint. According to this configuration, in the binder component, the silanol and titanium compound in the hydrolysis product are easily combined to form a thin and uniform film with a high crosslinking density. In particular, it is thought that the part of the titanium compound that binds to an inorganic substance and the part that has an affinity for ethersilicate due to silanol are crosslinked synergistically. Therefore, the present coating material has good mechanical adhesion to the metal or glass surface constituting the element body of the electronic component to be coated. Paints made by mixing such binder components with inorganic fillers and, if necessary, inorganic pigments, have a baking temperature of 150°C or more.
A hardening process at 170°C and a baking time of 10 to 15 minutes results in dehydration and condensation, producing ceramic-like siloxane and forming a dense coating film without generating harmful gases. Description of Examples Examples of the present invention will be described below. First, as shown in Table 1 below, a binder was prepared by hydrolyzing 25 parts of aqueous colloidal silica (silica solid content 20%) and 5 parts of ethyl silicate monomer using 1 part and 2 parts of a titanate coupling agent as a catalyst. As components, 70 parts of an inorganic filler and 1 part of an inorganic pigment were mixed therewith to form a uniform liquid slurry into a paint. Table 1 also shows a comparative example in which the titanate coupling agent was 0 parts and the other proportions were the same as above. The coating film properties as a paint at this time are shown in Table 2 below.
【表】【table】
【表】【table】
【表】
上記3種類の塗料における電子部品としての被
覆塗料の性能(電気的性能及び機械的性能)を下
記の表3に示す。[Table] The performance (electrical performance and mechanical performance) of the coating paint as an electronic component in the above three types of paint is shown in Table 3 below.
【表】【table】
【表】
ここで、硬度等の特性は塗膜強度テストを除い
て第1図に示す供試抵抗体にて行つた。すなわ
ち、第1図で1は10mm×5mm×0.8mmのアルミナ
基板、2はその基板1の電極3,3間に設けられ
たRuO2系の抵抗体、4は上記塗料による塗装膜
である。また、第2図は塗膜強度テストの際の図
を示し、5は1mm厚の鉄板、6は上記塗料による
塗装膜(塗膜厚2mm)、7は上記塗装膜6中に埋
設された線径0.6mmの端子である。そして、塗膜
強度テストは端子7を矢印F方向に引張り、塗装
膜6が破壊に至るまでの耐抗力を測定した。ま
た、煮沸テストは沸騰水中に浸漬し、30分煮沸後
の抵抗値変化率であり、加圧蒸気テスト(スチー
ムクツカーテスト)は121℃,2気圧の水蒸気圧
中に供試抵抗体を100時間放置後の抵抗値変化率
で示した。さらに、耐溶剤性はクロロセンの溶剤
中に供試抵抗体を浸漬し、30分間超音波洗浄した
時の塗膜を鉛筆硬度で測定した。また、不燃性は
供試抵抗体に過負荷電力20Wを瞬時に印加し、抵
抗体2がオープンに至るまで通電することにより
観察した。さらに、耐湿負荷は60℃,95%(相対
湿度)の雰囲気中で1Wを供試抵抗体に連続通電
し、1000時間後の抵抗値変化率で測定した。そし
て、耐熱負荷は85℃の雰囲気中で1Wを供試抵抗
体に連続通電し、1000℃時間後の抵抗値変化率で
測定した。
これらの表2,表3に示されるように、本発明
塗料による実施例1,2の焼付塗膜は低温,短時
間の焼付硬化が可能であり、溶剤に侵されること
もなく、吸湿性に対する耐湿性にも優れ、かつ煮
沸や加圧蒸気(スチームクツカー)テストに対し
ても従来品以上の性能を示していることが解る。
特に、本不燃性塗料は焼付後ほとんど無機質から
なる塗膜が形成されるため、過負荷に対し発炎や
引火を伴わず、かつ耐熱性にも優れるため電子部
品としての安全性を十分確保しているといえる。
また、本塗料の溶媒は水であるため保管性,作業
性が良く、塗料取扱い時の塗料付着や汚れに対し
ても容易に水でふきとれることとなる。すなわ
ち、本発明は有機溶剤を使用しない無公害,無
毒,無臭の塗料を提供しているものである。
ここで、本発明塗料は上記実施例に限定される
ものではなく、シリカ固形成分1%〜40%を有す
る水性コロイダルシリカ1部〜30部,エチルシリ
ケート単量体1部〜5部,無機質フイラー50部〜
70部の範囲で所期の目的,効果を達成することが
できる。すなわち、水性コロイダルシリカは30部
を超えるとコロイダル液のゲル化が起つたり、塗
膜にクラツクが発生したりして安定性が悪くな
り、また水性コロイダルシリカは1部以上で効果
を発揮する。次に、水性コロイダルシリカのシリ
カ固形成分が0%(シリカなし)ではコロイダル
シリカを形成できないため不可であり、1%未満
でも焼付後の塗膜強度が劣化し、一方シリカ固形
成分が40%を超えた場合にはコロイダル液のゲル
化が始まつて好ましくない。また、エチルシリケ
ート単量体の限定理由は、エチルシリケートとは
シリコン水溶液であり、1部未満では結合力がな
くなり、5部を超えた時にはゲル化して塗膜にク
ラツクが発生するためである。さらに、無機質フ
イラーが70部を超えた場合には塗膜の柔軟性がな
くなり塗膜強度が劣化し、特に煮沸に耐えられず
吸水率が著しく大きくなる。一方、無機質フイラ
ーが50部未満では粘りがなくなつて塗膜強度が劣
化する。また、チタネート系カツプリング剤の限
定理由は、1部未満では触媒効力がなく、3部を
超えた場合にはゲル化し塗膜にクラツクが発生す
るためである。なお、無機顔料は別段入れなくと
も良いものであるが、0部の場合には白色となつ
て外観上の汚れが目立ち易くなるため、適宜無機
顔料を入れてやる方が電子部品用としては実用上
好ましいものである。
発明の効果
以上のように本発明に係る電子部品用不燃性塗
料は構成されているものであり、低温,かつ短時
間の焼付硬化が可能なため、量産性に富むと共に
省エネルギーの面でも有利なものである。また、
電子部品に被覆した際にその機械的な密着性が良
好で、耐溶剤性に優れ、しかも過負荷に対し発炎
や引火を伴わず、かつ耐熱性に優れているため電
子部品の被覆材としての安全性を十分確保するこ
とができるものである。そして、耐湿性等の品質
特性も良好で、かつ有機溶剤を使用しない無公
害,無毒,無臭の塗料を提供するものであり、そ
の産業性は誠に大なるものである。[Table] Here, properties such as hardness were measured using the test resistor shown in FIG. 1, except for the coating film strength test. That is, in FIG. 1, 1 is an alumina substrate of 10 mm x 5 mm x 0.8 mm, 2 is a RuO 2 -based resistor provided between electrodes 3 and 3 of the substrate 1, and 4 is a coating film made of the above-mentioned paint. In addition, Fig. 2 shows a diagram during a coating film strength test, where 5 is a 1 mm thick iron plate, 6 is a coating film made of the above paint (2 mm coating thickness), and 7 is a line buried in the above coating film 6. It is a terminal with a diameter of 0.6mm. In the coating film strength test, the terminal 7 was pulled in the direction of arrow F, and the resistance strength until the coating film 6 was destroyed was measured. In addition, the boiling test is the resistance change rate after immersing in boiling water for 30 minutes, and the pressurized steam test (steam cutter test) is the resistance value change rate after immersing the resistor in boiling water for 30 minutes. It is expressed as the rate of change in resistance value after standing for a period of time. Furthermore, the solvent resistance was measured by immersing the test resistor in a chlorocene solvent and cleaning it with ultrasonic waves for 30 minutes, and measuring the pencil hardness of the coating film. In addition, nonflammability was observed by instantaneously applying an overload power of 20 W to the resistor under test and conducting the current until the resistor 2 became open. Furthermore, the humidity resistance load was measured by continuously applying 1W to the resistor under test in an atmosphere of 60°C and 95% (relative humidity), and measuring the rate of change in resistance value after 1000 hours. The heat resistance load was measured by continuously applying 1W to the resistor under test in an atmosphere of 85°C, and measuring the rate of change in resistance value after 1000°C. As shown in Tables 2 and 3, the baked coating films of Examples 1 and 2 using the paints of the present invention can be cured by baking at low temperatures in a short time, are not attacked by solvents, and have excellent resistance to hygroscopicity. It can be seen that it has excellent moisture resistance and also shows better performance than conventional products in boiling and pressurized steam tests.
In particular, this nonflammable paint forms a coating film made mostly of inorganic materials after baking, so it does not cause flames or ignition when overloaded, and has excellent heat resistance, ensuring sufficient safety as an electronic component. It can be said that
Furthermore, since the solvent of this paint is water, it has good storage and workability, and paint adhesion and stains during handling of the paint can be easily wiped off with water. That is, the present invention provides a pollution-free, non-toxic, and odorless paint that does not use organic solvents. Here, the coating material of the present invention is not limited to the above examples, but includes 1 part to 30 parts of aqueous colloidal silica having a silica solid content of 1% to 40%, 1 part to 5 parts of ethyl silicate monomer, and an inorganic filler. 50 copies~
The desired purpose and effect can be achieved within the range of 70 copies. In other words, if the amount of water-based colloidal silica exceeds 30 parts, the colloidal liquid may gel, or cracks may occur in the coating film, resulting in poor stability, and water-based colloidal silica is not effective at more than 1 part. . Next, if the silica solid component of aqueous colloidal silica is 0% (no silica), it is impossible to form colloidal silica, and if it is less than 1%, the strength of the coating after baking will deteriorate, while on the other hand, if the silica solid component is 40% If it exceeds it, the colloidal liquid will begin to gel, which is not preferable. Further, the reason for limiting the amount of ethylsilicate monomer is that ethylsilicate is an aqueous silicone solution, and if it is less than 1 part, it will lose its binding strength, and if it exceeds 5 parts, it will gel and cause cracks in the coating film. Furthermore, if the amount of the inorganic filler exceeds 70 parts, the coating film loses its flexibility and its strength deteriorates, and in particular it cannot withstand boiling, resulting in a significantly high water absorption rate. On the other hand, if the amount of inorganic filler is less than 50 parts, the coating loses stickiness and the strength of the coating deteriorates. The titanate coupling agent is limited because if it is less than 1 part, it has no catalytic effect, and if it exceeds 3 parts, it will gel and cause cracks in the coating film. Note that it is not necessary to separately add inorganic pigments, but if it is 0 parts, the color will be white and stains will be more noticeable on the exterior, so it is better to add inorganic pigments as appropriate for practical use in electronic parts. This is particularly preferable. Effects of the Invention As described above, the nonflammable paint for electronic parts according to the present invention is constructed and can be baked and cured at low temperatures and in a short time, making it suitable for mass production and advantageous in terms of energy saving. It is something. Also,
It has good mechanical adhesion when coated on electronic parts, has excellent solvent resistance, does not cause flames or ignition under overload, and has excellent heat resistance, making it suitable as a coating material for electronic parts. It is possible to sufficiently ensure safety. Moreover, the present invention provides a pollution-free, non-toxic, and odor-free paint that has good quality characteristics such as moisture resistance, and does not use organic solvents, and has great industrial potential.
第1図、第2図はそれぞれ本発明塗料を被覆し
た供試品を示す説明図である。
4,6……塗料膜。
FIGS. 1 and 2 are explanatory diagrams showing a sample coated with the paint of the present invention, respectively. 4, 6...Paint film.
Claims (1)
イダルシリカ1部〜30部とエチルシリケート単量
体1部〜5部をチタネート系カツプリング剤1部
〜2部を触媒として加水分解させたものに無機質
フイラー50部〜70部を混合してなる電子部品用不
燃性塗料。1. 1 to 30 parts of aqueous colloidal silica having a silica solid content of 1% to 40% and 1 to 5 parts of ethyl silicate monomer are hydrolyzed using 1 to 2 parts of a titanate coupling agent as a catalyst to inorganic A nonflammable paint for electronic parts made by mixing 50 to 70 parts of filler.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2892383A JPS59155468A (en) | 1983-02-23 | 1983-02-23 | Nonflammable paint for electronic part |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2892383A JPS59155468A (en) | 1983-02-23 | 1983-02-23 | Nonflammable paint for electronic part |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59155468A JPS59155468A (en) | 1984-09-04 |
JPS6411074B2 true JPS6411074B2 (en) | 1989-02-23 |
Family
ID=12261917
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2892383A Granted JPS59155468A (en) | 1983-02-23 | 1983-02-23 | Nonflammable paint for electronic part |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59155468A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5639578A (en) * | 1995-06-07 | 1997-06-17 | Eveready Battery Company | Current collectors for alkaline cells |
-
1983
- 1983-02-23 JP JP2892383A patent/JPS59155468A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59155468A (en) | 1984-09-04 |
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