JPS6249317B2 - - Google Patents

Info

Publication number
JPS6249317B2
JPS6249317B2 JP10374079A JP10374079A JPS6249317B2 JP S6249317 B2 JPS6249317 B2 JP S6249317B2 JP 10374079 A JP10374079 A JP 10374079A JP 10374079 A JP10374079 A JP 10374079A JP S6249317 B2 JPS6249317 B2 JP S6249317B2
Authority
JP
Japan
Prior art keywords
iron
added
water
reaction
metal
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
JP10374079A
Other languages
Japanese (ja)
Other versions
JPS5628276A (en
Inventor
Kunio Hirao
Shuji Hatsutori
Seiji Kamiharashi
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 JP10374079A priority Critical patent/JPS5628276A/en
Publication of JPS5628276A publication Critical patent/JPS5628276A/en
Publication of JPS6249317B2 publication Critical patent/JPS6249317B2/ja
Granted legal-status Critical Current

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  • Thermotherapy And Cooling Therapy Devices (AREA)

Description

【発明の詳細な説明】 最近、鉄の酸化反応時の生成熱を利用した使い
捨てタイプの懐炉が旅行、レジヤー用として市場
で人気を得ている。これらに利用されている発熱
組成物は、主成分である鉄粉に金属の塩化物ある
いは硫酸塩を反応助成物として添加し、水および
酸素と反応させて発熱させるものである。しか
し、これらの発熱組成物は反応初期の温度特性を
得るために、主成分である鉄と、反応助成物とし
て使用する金属の塩化物あるいは硫酸塩の金属イ
オンのイオン化傾向による交換反応を利用するた
め、(例えばFe゜+Cu++→Fe+++Cu゜)反応助成
物として利用できる金属塩は著しく制限を受け、
かつこれらの金属塩は一般に貴な金属であること
からコストが高いという問題点を有している。ま
た塩化物あるいは硫酸塩を構成する金属において
鉄よりもイオン化傾向が大なる金属では初期の交
換反応は行なわれず、温度特性が著しく悪く、発
熱剤としての効能を発揮し得ない。
DETAILED DESCRIPTION OF THE INVENTION Recently, disposable type hand warmers that utilize the heat generated during the oxidation reaction of iron have become popular in the market for travel and leisure use. The exothermic compositions used in these applications are those in which a metal chloride or sulfate is added as a reaction aid to iron powder, which is the main component, and the mixture reacts with water and oxygen to generate heat. However, in order to obtain the temperature characteristics at the initial stage of the reaction, these exothermic compositions utilize an exchange reaction between the main component iron and the ionization tendency of the metal ion of the metal chloride or sulfate used as a reaction aid. Therefore, the metal salts that can be used as reaction aids (for example, Fe゜+Cu ++ →Fe +++ Cu゜) are severely limited.
Moreover, since these metal salts are generally noble metals, they have the problem of high cost. Furthermore, among the metals constituting the chloride or sulfate, if the metal has a greater ionization tendency than iron, the initial exchange reaction will not take place, the temperature characteristics will be extremely poor, and the metal will not be effective as a heat generating agent.

本発明は上記の点に鑑み、水溶性ヒドラジン無
機酸塩を反応開始剤として添加し、かつ金属の酸
化物を補助の反応組成物として添加することによ
り、発熱温度が高く、かつ発熱時間も長い発如組
成物を提供するものである。
In view of the above points, the present invention provides a high exothermic temperature and a long exothermic time by adding a water-soluble hydrazine inorganic acid salt as a reaction initiator and adding a metal oxide as an auxiliary reaction composition. The present invention provides an instant composition.

以下、本発明の詳細について説明する。本発明
の発熱組成物の主成分である鉄については発熱が
可能な鉄材であればよく、形状としては粉体、粒
体などが使用される。また反応助成物としての金
属の塩化物あるいは硫酸塩は高純度のものを使用
する必要はなく、その添加量は鉄100重量部に対
して0.5〜20重量部程度である。この場合、コス
トの安いアルカリ金属やアルカリ土類金属の塩を
用いればよく、また海水等を加えることも可能で
ある。
The details of the present invention will be explained below. Iron, which is the main component of the heat generating composition of the present invention, may be any iron material that can generate heat, and may be in the form of powder, granules, etc. Furthermore, it is not necessary to use a highly pure metal chloride or sulfate as a reaction aid, and the amount added is approximately 0.5 to 20 parts by weight per 100 parts by weight of iron. In this case, inexpensive alkali metal or alkaline earth metal salts may be used, and seawater or the like may also be added.

また反応開始剤としての水溶性ヒドラジン無機
酸塩および補助の反応助成物としての金属の酸化
物は、特に高純度のものを使用する必要はなく、
その添加量は鉄100重量部に対して水溶性ヒドラ
ジン無機酸塩は0.5重量部以上で、かつ金属の酸
化物は1〜20重量部で充分である。
Furthermore, the water-soluble hydrazine inorganic acid salt as a reaction initiator and the metal oxide as an auxiliary reaction aid do not need to be of particularly high purity.
It is sufficient to add 0.5 parts by weight or more of the water-soluble hydrazine inorganic acid salt and 1 to 20 parts by weight of the metal oxide per 100 parts by weight of iron.

また水としては一般に用いられているものであ
ればよく、その添加量は鉄100重量部に対して10
〜100重量部であり、この場合、海水も可能であ
る。また水を含浸し得る保水材としての素灰、活
性炭などの炭素、シリカゲル、木粉などの添加量
は鉄100重量部に対して10〜100重量部が最適であ
る。
In addition, any commonly used water may be used, and the amount added is 10 parts by weight per 100 parts by weight of iron.
~100 parts by weight, in which case seawater is also possible. The optimal amount of water-retaining materials that can be impregnated with water, such as raw ash, carbon such as activated carbon, silica gel, and wood powder, is 10 to 100 parts by weight per 100 parts by weight of iron.

さらに酸素としては一般的に空気を用いる。 Furthermore, air is generally used as oxygen.

次に本発明の発熱組成物を懐炉として応用した
場合の実施例について説明する。まず発熱組成物
を入れる袋は、不織布の内面を厚さ30μのポリエ
チレンシートでラミネートした大きさが120×85
mmのものを用いた。また発熱組成物の混合比は鉄
粉30g、保水材として素灰10g、反応開始剤とな
る水溶性ヒドラジン無機酸塩として塩酸ヒドラジ
ン0.5g、水15c.c.、金属の酸化物として酸化銅1.5
g、鉄よりもイオン化傾向が大なる金属の塩化物
としてNacl2gである。これらの混合物を上記袋
に入れ、そして袋の開口部をヒートシールにより
密封し、懐炉としての発熱特性(発熱温度−発熱
時間特性)を測定した。この場合、発熱温度の測
定は銅コンスタンタン熱電対を用い、気温25℃、
湿度45%RHの恒温恒湿室で行なつた。
Next, an example in which the exothermic composition of the present invention is applied as a hand warmer will be described. First, the bag to contain the exothermic composition is made of a non-woven fabric laminated with a 30μ thick polyethylene sheet and has a size of 120 x 85 mm.
mm was used. The mixing ratio of the exothermic composition is 30 g of iron powder, 10 g of raw ash as a water retaining material, 0.5 g of hydrazine hydrochloride as a water-soluble hydrazine inorganic acid salt serving as a reaction initiator, 15 c.c. of water, and 1.5 g of copper oxide as a metal oxide.
g, Nacl2g is a metal chloride that has a greater ionization tendency than iron. These mixtures were placed in the bag, and the opening of the bag was sealed by heat sealing, and the heat generation characteristics (heat generation temperature - heat generation time characteristics) as a hand warmer were measured. In this case, the heat generation temperature was measured using a copper constantan thermocouple at an air temperature of 25°C.
The experiments were conducted in a constant temperature and humidity room with a humidity of 45% RH.

なお、第1図は反応開始剤を添加しない場合A
と、反応開始剤は添加しているが、酸化銅は添加
していない場合Bと、反応開始剤、酸化銅とも添
加した場合Cの発熱特性の比較を示したもので、
この第1図からも明らかなように、反応開始剤を
添加しない場合Aは、発熱が始まるのが遅く、か
つ発熱温度も低く、発熱剤としての効果はほとん
どない。また酸化銅を添加していない場合Bは、
酸化銅を添加している場合Cに比べ、若干発熱温
度が低く、かつ初期の温度特性も悪い。
In addition, Figure 1 shows A when no reaction initiator is added.
This shows a comparison of the exothermic properties of B, where a reaction initiator is added but no copper oxide, and C, where both a reaction initiator and copper oxide are added.
As is clear from FIG. 1, in the case where no reaction initiator is added, the heat generation starts slowly and the heat generation temperature is low, so that it has almost no effect as an exothermic agent. In addition, in case B does not contain copper oxide,
When copper oxide is added, the exothermic temperature is slightly lower than that of C, and the initial temperature characteristics are also poor.

第2図は従来使用されている塩化銅を反応助成
物として用いている従来品Dと、上記本発明の実
施例品Eとの低温時における発熱特性の比較を示
したもので、この第2図からも明らかなように、
従来品Dは懐炉として使用した場合の適温範囲X
(45℃〜65℃)が得られる時間は約5時間程度で
あるのに対し、本発明の実施例品Eは約10時間以
上である。このことからも、本発明の実施例品E
は低温においても性能が優れており、特に寒冷地
や冬期の屋外での使用に有効である。またこの低
温の発熱温度の測定は銅コンスタンタン熱電対を
用い、気温5℃、湿度60%RHの恒温恒湿室で行
なつた。
Figure 2 shows a comparison of the exothermic properties at low temperatures between conventional product D, which uses conventionally used copper chloride as a reaction aid, and the above-mentioned example product E of the present invention. As is clear from the figure,
Conventional product D has an appropriate temperature range X when used as a pocket warmer.
(45°C to 65°C) is about 5 hours, whereas Example Product E of the present invention takes about 10 hours or more. From this, it can be seen that Example product E of the present invention
It has excellent performance even at low temperatures, and is particularly effective for use in cold regions and outdoors during the winter. The low-temperature heat generation temperature was measured using a copper constantan thermocouple in a constant temperature and humidity room with an air temperature of 5°C and a humidity of 60% RH.

なお、上記実施例においては、金属の酸化物と
した酸化銅を用いたものについて説明したが、こ
れ以外としてはマンガン、クロム、カルシウム、
コバルト、ニツケル、マグネシウムの酸化物が有
効であり、これらを単独あるいは複数の混合物と
して添加しても上記実施例と同様の作用効果を奏
するものである。
In the above example, copper oxide was used as a metal oxide, but other examples include manganese, chromium, calcium,
Oxides of cobalt, nickel, and magnesium are effective, and even if they are added alone or as a mixture of a plurality of them, the same effects as in the above embodiments can be obtained.

以上のように本発明の発熱組成物は、水溶性ヒ
ドラジン無機酸塩を反応開始剤として添加し、か
つ金属の酸化物を補助の反応助成物として添加し
ているため、発熱の立ち上がりが速く、かつ発熱
温度も高く、しかも懐炉として使用した場合の適
温範囲の得られる発熱時間も長い等種々優れた特
長を有する。
As described above, in the exothermic composition of the present invention, the water-soluble hydrazine inorganic acid salt is added as a reaction initiator, and the metal oxide is added as an auxiliary reaction aid, so that the exothermic composition quickly generates heat. It also has various excellent features, such as a high heat generation temperature and a long heat generation time that provides an appropriate temperature range when used as a hand warmer.

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

第1図は本発明の実施例品と、酸化銅を添加し
ていないものあるいは反応開始剤を添加していな
いものとの発熱特性の比較を示すグラフ、第2図
は従来品と本発明の実施例品との低温時における
発熱特性の比較を示すグラフである。
Figure 1 is a graph showing a comparison of exothermic characteristics between the example product of the present invention and the product without copper oxide or reaction initiator added, and Figure 2 is a graph showing the comparison between the conventional product and the product of the present invention. It is a graph showing a comparison of heat generation characteristics at low temperatures with Example products.

Claims (1)

【特許請求の範囲】 1 鉄と、鉄よりもイオン化傾向の大きな金属の
塩化物または硫酸塩を有効成分とし、かつこの有
効成分に金属の酸化物を補助の反応助成物として
添加するとともに、水溶性ヒドラジン無機酸塩を
反応開始剤として添加し、水および酸素と反応し
て発熱することを特徴とする発熱組成物。 2 前記金属の酸化物は銅、マンガン、クロム、
カルシウム、コバルト、ニツケル、マグネシウム
からなる群の酸化物であつて、これらを単独ある
いは複数の混合物として添加してなる特許請求の
範囲第1項記載の発熱組成物。
[Scope of Claims] 1 Iron and a chloride or sulfate of a metal with a greater ionization tendency than iron are used as active ingredients, and a metal oxide is added to this active ingredient as an auxiliary reaction aid, and a water-soluble 1. A heat-generating composition containing a hydrazine inorganic acid salt as a reaction initiator, which reacts with water and oxygen to generate heat. 2 The oxides of the metals include copper, manganese, chromium,
2. The exothermic composition according to claim 1, which is an oxide of the group consisting of calcium, cobalt, nickel, and magnesium, and is added singly or as a mixture of a plurality of these.
JP10374079A 1979-08-15 1979-08-15 Pyrogenic composition Granted JPS5628276A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10374079A JPS5628276A (en) 1979-08-15 1979-08-15 Pyrogenic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10374079A JPS5628276A (en) 1979-08-15 1979-08-15 Pyrogenic composition

Publications (2)

Publication Number Publication Date
JPS5628276A JPS5628276A (en) 1981-03-19
JPS6249317B2 true JPS6249317B2 (en) 1987-10-19

Family

ID=14362006

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10374079A Granted JPS5628276A (en) 1979-08-15 1979-08-15 Pyrogenic composition

Country Status (1)

Country Link
JP (1) JPS5628276A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8902997B2 (en) 2009-06-03 2014-12-02 Nippon Telegraph And Telephone Corporation PARCOR coefficient quantization method, PARCOR coefficient quantization apparatus, program and recording medium

Also Published As

Publication number Publication date
JPS5628276A (en) 1981-03-19

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