JPH02281565A - Thermal cell - Google Patents
Thermal cellInfo
- Publication number
- JPH02281565A JPH02281565A JP10382489A JP10382489A JPH02281565A JP H02281565 A JPH02281565 A JP H02281565A JP 10382489 A JP10382489 A JP 10382489A JP 10382489 A JP10382489 A JP 10382489A JP H02281565 A JPH02281565 A JP H02281565A
- Authority
- JP
- Japan
- Prior art keywords
- heating agent
- pad
- ignition
- ignition pad
- battery
- 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
Links
- 238000010438 heat treatment Methods 0.000 claims abstract description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 26
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 claims description 4
- 229940083898 barium chromate Drugs 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 2
- AXZAYXJCENRGIM-UHFFFAOYSA-J dipotassium;tetrabromoplatinum(2-) Chemical compound [K+].[K+].[Br-].[Br-].[Br-].[Br-].[Pt+2] AXZAYXJCENRGIM-UHFFFAOYSA-J 0.000 claims description 2
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 229910001487 potassium perchlorate Inorganic materials 0.000 claims description 2
- 229910052726 zirconium Inorganic materials 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 abstract description 9
- 238000002485 combustion reaction Methods 0.000 description 12
- 239000011810 insulating material Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003792 electrolyte Substances 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000010248 power generation Methods 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 1
- 235000016796 Euonymus japonicus Nutrition 0.000 description 1
- 240000006570 Euonymus japonicus Species 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000009841 combustion method Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000003411 electrode reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000005338 heat storage Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910000339 iron disulfide Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- NIFIFKQPDTWWGU-UHFFFAOYSA-N pyrite Chemical compound [Fe+2].[S-][S-] NIFIFKQPDTWWGU-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
Classifications
-
- 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
- H01M6/30—Deferred-action cells
- H01M6/36—Deferred-action cells containing electrolyte and made operational by physical means, e.g. thermal cells
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Primary Cells (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明はリチウム/二硫化鉄系熱電池における内部リー
ド板間の絶縁性の向上に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application This invention relates to improving the insulation between internal lead plates in a lithium/iron disulfide thermal battery.
従来の技術
熱電池は常温で不活性であるが、高温に加熱すると活性
となり、外部へ電力を供給し得るようになる電池で貯蔵
形電池の一種である。従って、6〜10年あるいはそれ
以上の貯蔵後においても製造直後と何ら電池特性が変ら
ないので緊急用電源に利用されている。また、高温で作
動させるために電極反応が進み易いため分極も少ないの
で大電流放電性に優れ、さらに使用希望時には起動信号
を入れると瞬時に電力を取出せる等の特徴を有する。BACKGROUND TECHNOLOGY A thermal battery is inactive at room temperature, but becomes active when heated to a high temperature and can supply power to the outside, and is a type of storage battery. Therefore, even after storage for 6 to 10 years or more, the battery characteristics remain the same as they were immediately after manufacture, so they are used as an emergency power source. In addition, since it is operated at high temperatures, electrode reactions can easily proceed, so there is little polarization, so it has excellent large current discharge properties, and when desired, it has features such as instantaneous power extraction when a start signal is input.
この種の電池は内部に発熱剤を内蔵するものが多く1発
熱剤により発生する熱により常温では固体でイオン伝導
性のない溶融塩を溶融し電池として活性化されるもので
ある。Most of these types of batteries have a heat generating agent built in, and the heat generated by the heat generating agent melts a molten salt that is solid at room temperature and has no ion conductivity, and is activated as a battery.
第3図を用いて、従来形熱電池の構造を説明する。図中
1は素電池、2は加熱剤であり、これらを交互に積層し
た発電部分の上下両端部には放熱を緩和させ、長時間に
わたって作動温度を保持する蓄熱層3が配されている。The structure of a conventional thermal battery will be explained using FIG. In the figure, 1 is a unit cell, 2 is a heating agent, and a heat storage layer 3 is arranged at both upper and lower ends of a power generation part in which these are laminated alternately to moderate heat radiation and maintain an operating temperature for a long time.
この積層体の上端部に素電池、加熱剤と同径の着火パフ
ドロと、点火器4が構成されている。積層体の側部に導
火帯5があり、この導火帯と重ならない位置に正極り一
ド板8′、負極リード板9′が積層体最上部および最下
部から引出され、正極端子8.負極端子9に溶接されて
いる。その他の構成部品として、一対の点火器外部端子
7.断熱材12を有し、外装蓋1゜と外装ケー711の
嵌合部を溶接して積層体を一定圧力で保持する。A unit cell, an ignition puff drum having the same diameter as the heating agent, and an igniter 4 are constructed at the upper end of this laminate. There is a fuse cord 5 on the side of the stack, and a positive electrode lead plate 8' and a negative electrode lead plate 9' are pulled out from the top and bottom of the stack at positions that do not overlap with the fuse cord, and the positive terminal 8 is pulled out from the top and bottom of the stack. .. It is welded to the negative electrode terminal 9. Other components include a pair of igniter external terminals7. It has a heat insulating material 12, and the fitting portion of the outer cover 1° and the outer case 711 is welded to hold the stacked body at a constant pressure.
以上の様に構成された従来の熱電池について。Regarding the conventional thermal battery configured as above.
以下その動作を説明する。まず、点火器外部端子7から
微小電流が通電されると点火器4から小さな火炎が発生
する。この小さな火炎は着火バフドロを燃焼して大きな
火種となって導火帯6を燃焼させ、素電池間の加熱剤2
に着火、燃焼伝ばし。The operation will be explained below. First, when a minute current is applied from the igniter external terminal 7, a small flame is generated from the igniter 4. This small flame burns the ignited buff mud, becomes a large spark, burns the fuse cord 6, and heats the heating agent 2 between the cells.
ignition and combustion spread.
高速にかつ大量に発熱反応を起こして素電池1を加熱す
る。素電池は400〜700℃に昇温されて電解質が溶
融し、放電開始状態となシ正、負極端子8.9から電圧
、電流を出力する。着火パッドはジルコニウム(Zr)
とクロム酸バリウム(BaCrO4)の混合物から成り
、燃焼直後の赤熱状態では電気伝導性を有するが、11
1以下で冷却し絶縁状態となる。また、両極のリード板
は積層体側部に密着するので、素電池と直接接触しない
よう絶縁部材や耐熱断熱材で覆っている。The unit cell 1 is heated by causing an exothermic reaction at high speed and in large quantities. The temperature of the unit cell is raised to 400 to 700° C., the electrolyte is melted, and the cell enters a discharge start state, outputting voltage and current from the positive and negative terminals 8.9. The ignition pad is zirconium (Zr)
and barium chromate (BaCrO4), and has electrical conductivity in the red-hot state immediately after combustion, but 11
When it is below 1, it cools down and becomes insulated. Furthermore, since the lead plates of both poles are in close contact with the sides of the laminate, they are covered with an insulating member or a heat-resistant heat insulating material so that they do not come into direct contact with the unit cells.
発明が解決しようとする課題
しかしながら上記の構成では、リード板に絶縁部材で保
護していても、起動時に着火パッドが燃焼してその反応
生成物が外周方向に変形して拡がり、その燃焼熱(約2
000°C)にて絶縁部材及び断熱材を破壊してしまっ
て、数十〜数百オームの導電性を有するようになる。そ
の反応残査は直接リード板と接触して、正極と負極間で
着火パッド反応残査を介して内部放電回路を形成すると
いう問題点を有していた。そこでこの問題点を解決する
ため、従来は第4図に示す点火器の真下にある着火パッ
ドを取シ除き、燃焼による変形のほとんどない加熱剤を
直接配するという構成を行っていた。しかしながらこの
場合内部放電回路の形成はないが1点火トリガーを入れ
てから規定電圧に到達する立ち上がシ時間が1706!
iから320m5へと2倍近く遅くなってしまうという
問題が起こった。Problems to be Solved by the Invention However, in the above configuration, even if the lead plate is protected by an insulating member, the ignition pad burns during startup, and the reaction products are deformed and spread in the outer circumferential direction, and the combustion heat ( Approximately 2
000°C), the insulating member and heat insulating material are destroyed, and the electrical conductivity becomes several tens to hundreds of ohms. There was a problem in that the reaction residue directly contacted the lead plate and formed an internal discharge circuit between the positive electrode and the negative electrode via the ignition pad reaction residue. In order to solve this problem, the conventional construction was to remove the ignition pad located directly below the igniter as shown in FIG. 4, and directly place the heating agent, which is hardly deformed by combustion. However, in this case, although no internal discharge circuit is formed, it takes 1706 seconds to reach the specified voltage after turning on the ignition trigger!
A problem arose in that the speed was almost twice as slow from i to 320m5.
本発明は上記従来の問題点を解決するもので。The present invention solves the above-mentioned conventional problems.
立ち上がり時間を損なわず、電池起動時に内部放電回路
を形成しない高召頼性の熱電池を提供することを目的と
する。To provide a highly reliable thermal battery that does not impair startup time and does not form an internal discharge circuit when starting the battery.
課題を解決するための手段
この目的を達成するために本発明は1点火器と、鉄と過
塩素酸カリウムの混合物からなる加熱剤と。Means for Solving the Problems To achieve this object the invention provides an igniter and a heating agent consisting of a mixture of iron and potassium perchlorate.
ジルコニウムとクロム酸バリウムの混合物からなる従来
と同材料の着火パッドを用い、前記着火パッドの外径を
素電池および加熱剤径よシも70%から90%の範囲で
小径とし、かつ両者の寸法差が10H以内に小さくシ、
更に1着火パッドと加熱剤とが接するようにしたもので
ある。An ignition pad made of the same material as the conventional one consisting of a mixture of zirconium and barium chromate is used, and the outer diameter of the ignition pad is made smaller within the range of 70% to 90% of the diameter of the unit cell and the heating agent, and the dimensions of both are small. The difference is small within 10H,
Furthermore, one ignition pad and the heating agent are in contact with each other.
作用
この構成によれば、燃焼後の着火パッド反応残査が、加
熱剤の反応物と一体となって拡がり難くなシ、従って、
正・負極リードの絶縁部材の損傷が少なく、かつこの間
に隙間ができて接触し難く出来る。これらの理由で高熱
の燃焼熱が発生しても絶縁部材の破壊によって着火パッ
ドの反応残査に導電性を与えることがなく、内部放電回
路を形成する現象は防止できる。また1本発明は従来構
造をベースとして採用できるので、何ら技術的な困難を
伴なわない。従って、製造容易で、立上り時間への遅延
もなく、信頼性に優れた熱電池が構成できることとなる
。Effect: According to this configuration, the reaction residue of the ignition pad after combustion is difficult to spread together with the reactant of the heating agent, and therefore,
There is little damage to the insulating members of the positive and negative electrode leads, and there is a gap between them, making it difficult to contact them. For these reasons, even if high combustion heat is generated, the breakdown of the insulating member will not impart conductivity to the reaction residue of the ignition pad, and the phenomenon of forming an internal discharge circuit can be prevented. Furthermore, since the present invention can be adopted based on the conventional structure, it does not involve any technical difficulties. Therefore, it is possible to construct a thermal battery that is easy to manufacture, has no delay in start-up time, and has excellent reliability.
実施例
以下本発明の実施例について1図面を参照しながら説明
する。EXAMPLE Hereinafter, an example of the present invention will be described with reference to one drawing.
(実施例1)
第1図は、従来の着火パッドを小径とした改良着火パク
ド13を用い、その下側に設けた加熱剤2と接触させた
構造の熱電池で、その他の構成部品は第3図の従来例と
同一構成である。本構成の特徴は、直径45mの改良着
火パッド13から直接に導火帯6に燃焼伝ばさせるので
はなく、直径esowの加熱剤2へ伝ばし、加熱剤2を
介して行なわせる様にしたところにある。こうすること
により、改良着火パッドの反応残査が加熱剤の反応残査
と一体となって、固定され拡がり難くなり絶縁部材を破
壊しにくくなる。(Example 1) Fig. 1 shows a thermal battery with a structure in which an improved ignition pad 13 with a smaller diameter than the conventional ignition pad is brought into contact with a heating agent 2 provided below. It has the same configuration as the conventional example shown in FIG. The feature of this configuration is that combustion is not transmitted directly from the improved ignition pad 13 with a diameter of 45 m to the fuse cord 6, but is transmitted to the heating agent 2 with a diameter of esow, and is carried out via the heating agent 2. It's right there. By doing so, the reaction residue of the improved ignition pad becomes one with the reaction residue of the heating agent, becomes fixed and difficult to spread, and becomes difficult to destroy the insulating member.
(実施例2)
第2図は1本発明の他の実施例における熱電池の断面図
で、基本構成は前記第1図とほぼ同じである。本例の特
徴は、直径40ffの改良着火パッド13が外径5Qj
l1g、内径4oHのドーナツ状加熱剤14の内側に配
置され、厚み部分で接触し。(Embodiment 2) FIG. 2 is a sectional view of a thermal battery according to another embodiment of the present invention, and the basic configuration is almost the same as that of FIG. 1. The feature of this example is that the improved ignition pad 13 with a diameter of 40ff has an outer diameter of 5Qj.
It is placed inside the donut-shaped heating agent 14 with an inner diameter of 4oH, and is in contact with the thick part.
燃焼法ばさせていく方式で、さらに改良着火パッドから
発せられる高熱の燃焼熱の影響を抑制したところにある
。従って、よシ確実に絶縁部材や断熱材への影響を小さ
くできる。It is a method that spreads the combustion method, and the effect of the high-temperature combustion heat emitted from the improved ignition pad is further suppressed. Therefore, the influence on insulating members and heat insulating materials can be reduced more reliably.
上記実施例1.2の立上り時間は、0.468fl/m
sの高速燃焼スピードを有する着火パッドの外径が小さ
くなシ、その分を0.117ff/!Ilsの加熱剤が
おぎなうので1点火器が火炎を放ってから。The rise time of Example 1.2 above is 0.468 fl/m
The outer diameter of the ignition pad, which has a high combustion speed of s, is small, so it is 0.117ff/! After the igniter releases a flame as the Ils heating agent burns.
最下端の加熱剤が燃焼し終るまでの時間は、実施例1で
1ems、実施例2で321n8遅くなる。しかし、こ
の程度の遅延は実用的に問題とならず、発電開始までの
時間は、それぞれの燃焼スピードと燃焼長さの積を積算
した値と、素電池中の電解質溶融時間と、積層体層間の
伝熱スピードによるので、さらに緩和される。これによ
シ、素電池直径501ff、積層体高さ80101の電
池20個ずつの平均立上り時間と放電持続時間は下記の
結果となった。The time it takes for the heating agent at the bottom to finish burning is delayed by 1 ems in Example 1 and by 321n8 in Example 2. However, this degree of delay is not a practical problem, and the time until power generation starts depends on the product of the combustion speed and combustion length, the melting time of the electrolyte in the unit cell, and the gap between the layers of the stack. It is further relaxed because it depends on the heat transfer speed. As a result, the average rise time and discharge duration of 20 batteries each having a cell diameter of 501 ff and a laminate height of 80101 were as follows.
放電持続時間は1本実施例の場合いずれも大幅に改善さ
れておシ、従来例1との比較において約1.6倍となっ
ていることから、正極リード板と負極リード板の絶縁が
保持され、内部放電回路の形成が防止できたと推定でき
る。The discharge duration was significantly improved in each of the examples, and was approximately 1.6 times longer than in conventional example 1, indicating that the insulation between the positive and negative lead plates was maintained. Therefore, it can be assumed that the formation of an internal discharge circuit could be prevented.
改良着火パッドの寸法は1種々実験条件を変化させて確
認したところ、実施例1において、加熱剤外径寸法に対
し1片側5H以上すなわち直径で10M以上にする必要
はなく、最小3mm以上あれば信頼性を保てる。また、
加熱剤寸法と改良着火パッドの寸法比率では、上記条件
を満たし、改良着火パッドが70%以上小さくすると、
立上り時間や着火性に不利となり、90%以上大きくす
ると、絶縁部材への影響によりバラツキが多く発生した
。The dimensions of the improved ignition pad were confirmed by changing various experimental conditions, and in Example 1, it was not necessary to make the outer diameter of the heating agent 5H or more on one side, that is, 10M or more in diameter, as long as it was at least 3mm. Maintain reliability. Also,
If the heating agent size and the improved ignition pad size ratio satisfy the above conditions and the improved ignition pad is 70% or more smaller,
This was disadvantageous in rise time and ignitability, and when it was increased by 90% or more, many variations occurred due to the influence on the insulating member.
発明の効果
本発明は以上の説明からも明らかなように、加熱剤の外
径と改良着火パッドの外径比率が70%〜90%の範囲
内であり1両者の寸法差が最大値10ff以内、最小値
3111以上の関係で構成した熱電池は、着火パッドの
変形と、高熱の燃焼熱による絶縁部材や断熱材の損傷が
軽減されるようになるので、正極リード板と負極リード
板の内部放電回路の形成がなくなり、その効果として持
続時間が延長できる。更に、立上り時間への影響も若干
で済むため、実用的な問題とならない。Effects of the Invention As is clear from the above description, the present invention provides a method in which the ratio of the outer diameter of the heating agent to the outer diameter of the improved ignition pad is within the range of 70% to 90%, and the dimensional difference between the two is within the maximum value of 10ff. , a thermal battery configured with a minimum value of 3111 or more reduces deformation of the ignition pad and damage to insulating members and heat insulating materials due to high-temperature combustion heat. The formation of a discharge circuit is eliminated, and as a result, the duration can be extended. Furthermore, since the rise time is only slightly affected, this does not pose a practical problem.
従って、信頼性が高く、若干の手直し程度で立上り時間
も早く。かつ持続時間の改善された熱電池を提供するこ
とが出来るという効果が得られる。Therefore, it is highly reliable and has a quick start-up time with only minor modifications. Moreover, it is possible to provide a thermal battery with improved duration.
第1図、第2図は本発明の実施例における熱電池の縦断
面図、第3図、第4図は従来の熱電池の縦断面図である
。
2・・・・・・加熱剤、4・・・・・・点火器、5・・
・・・・導火帯。
8′・・・・・・正極リード板、9′・・・・・・負極
リード板、13・・・・・・改良着火パッド、14・・
・・・・ドーナツ状加熱剤。
代理人の氏名 弁理士 粟 野 重 孝 ほか1名f・
−・4む之
トー正希を畠)
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ト・−7+]%剤
3−1外層
8′−−一正1にり°Y本配
9−貧罹綿1
1−−一累電硬
2−即井豹
s−1@4
トー正騒を眉李
Il−・−外第ピ1ス
f・−1電だ
1−710弗劉
q−・kで錦壬
to−−−9LX菖
n −一タL装γ−ス1 and 2 are longitudinal sectional views of a thermal battery according to an embodiment of the present invention, and FIGS. 3 and 4 are longitudinal sectional views of a conventional thermal battery. 2... heating agent, 4... igniter, 5...
...Fuse cord. 8'... Positive electrode lead plate, 9'... Negative electrode lead plate, 13... Improved ignition pad, 14...
...Doughnut-shaped heating agent. Name of agent: Patent attorney Shigetaka Awano and 1 other person f.
-・4munoto Masaki wo Hatake) +-[1 possible・-7+]% agent 3-1 outer layer 8'--Kazumasa 1 degree Y main layer 9-poor cotton 1 1--1 1-710 Yuliu q--k to Geummi to--- 9LX iris n-ichita L γ-s
Claims (1)
剤と、ジルコニウムとクロム酸バリウムの混合物からな
る着火パッドとを有する熱電池において、前記着火パッ
ドの外径が加熱剤外径よりも寸法で最小3mm以上、最
大10mm以内の範囲で小さく、かつ、その比率で70
%〜90%の範囲内であり、かつ両者が接触しているこ
とを特徴とする熱電池。In a thermal battery having an igniter, a heating agent made of a mixture of iron and potassium perchlorate, and an ignition pad made of a mixture of zirconium and barium chromate, the outer diameter of the ignition pad is smaller than the outer diameter of the heating agent. The minimum size is 3mm or more and the maximum size is 10mm or less, and the ratio is 70mm.
% to 90%, and both are in contact.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10382489A JP2808652B2 (en) | 1989-04-24 | 1989-04-24 | Thermal battery |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10382489A JP2808652B2 (en) | 1989-04-24 | 1989-04-24 | Thermal battery |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02281565A true JPH02281565A (en) | 1990-11-19 |
JP2808652B2 JP2808652B2 (en) | 1998-10-08 |
Family
ID=14364163
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10382489A Expired - Lifetime JP2808652B2 (en) | 1989-04-24 | 1989-04-24 | Thermal battery |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2808652B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2475898C1 (en) * | 2011-11-10 | 2013-02-20 | Открытое акционерное общество "Энергия" | Thermal lithium current source |
RU2543069C2 (en) * | 2013-03-14 | 2015-02-27 | Открытое акционерное общество "Энергия" | Tiny thermal lithium current source |
RU193576U1 (en) * | 2019-07-09 | 2019-11-06 | Акционерное общество "Энергия" (АО "Энергия") | THERMAL CHEMICAL SOURCE |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2448393C1 (en) * | 2011-02-01 | 2012-04-20 | Открытое акционерное общество "Энергия" | Thermal chemical current source |
-
1989
- 1989-04-24 JP JP10382489A patent/JP2808652B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2475898C1 (en) * | 2011-11-10 | 2013-02-20 | Открытое акционерное общество "Энергия" | Thermal lithium current source |
RU2543069C2 (en) * | 2013-03-14 | 2015-02-27 | Открытое акционерное общество "Энергия" | Tiny thermal lithium current source |
RU193576U1 (en) * | 2019-07-09 | 2019-11-06 | Акционерное общество "Энергия" (АО "Энергия") | THERMAL CHEMICAL SOURCE |
Also Published As
Publication number | Publication date |
---|---|
JP2808652B2 (en) | 1998-10-08 |
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