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JPS6324030B2 - - Google Patents
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JPS6324030B2 - - Google Patents

Info

Publication number
JPS6324030B2
JPS6324030B2 JP54076113A JP7611379A JPS6324030B2 JP S6324030 B2 JPS6324030 B2 JP S6324030B2 JP 54076113 A JP54076113 A JP 54076113A JP 7611379 A JP7611379 A JP 7611379A JP S6324030 B2 JPS6324030 B2 JP S6324030B2
Authority
JP
Japan
Prior art keywords
water
metal
acid
reaction
heat
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
JP54076113A
Other languages
Japanese (ja)
Other versions
JPS561148A (en
Inventor
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 JP7611379A priority Critical patent/JPS561148A/en
Publication of JPS561148A publication Critical patent/JPS561148A/en
Publication of JPS6324030B2 publication Critical patent/JPS6324030B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】 最近、金属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、主成分である鉄粉などの金属に、金
属の硫酸塩あるいは塩化物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助成
物として金属塩を用いているため、使用廃棄後に
自然破懐を起こす危険率が高く、また一般にコス
トが高いなどの欠点を有するものである。さらに
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、主成分である金属と、反応助成物として
使用する金属の硫酸塩あるいは塩化物の金属イオ
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゜)主成分と
して用いる金属の種類は反応助成物として使用す
る金属イオンに著しく制限を受けるものである。
DETAILED DESCRIPTION OF THE INVENTION Recently, disposable type hand warmers that utilize the heat generated during the oxidation reaction of metals have become popular in the market for travel and leisure use. The heat-generating compositions used in these products are made by adding metal sulfate or chloride as a reaction aid to metal such as iron powder as the main component, and reacting with water and oxygen to generate heat. However, since these exothermic compositions use metal salts as reaction aids, they have drawbacks such as a high risk of spontaneous deterioration after use and disposal, and generally high costs. Furthermore, these exothermic compositions utilize an exchange reaction between the main component metal and the ionization tendency of the metal ion of the metal sulfate or chloride used as a reaction aid in order to obtain the temperature characteristics at the initial stage of the reaction. (For example, F e゜ + C u ++ → F e ++ + C u゜) The type of metal used as the main component is significantly limited by the metal ion used as a reaction aid.

本発明は上記問題点を解決するためになされた
もので、水素よりイオン化傾向が大なる金属すべ
てに対して有効であり、かつ自然破壊などの危険
が少ない水溶性有機酸を反応助成物として用いる
ことにより、従来品に比較して適温の得られる発
熱時間が長い優れた発熱組成物を提供するもので
ある。
The present invention was made to solve the above problems, and uses a water-soluble organic acid as a reaction aid, which is effective against all metals that have a greater tendency to ionize than hydrogen, and which has less risk of spontaneous destruction. This provides an excellent heat-generating composition that provides a suitable temperature and has a longer heat-generating time than conventional products.

以下、本発明の詳細について説明する。金属を
Mとし、かつCoHnをRとして、例えばカルボン
酸を反応助成物として用いた場合には次の反応式
(1)、(2)、(3)に示すように酸化反応が進行して生成
熱を発生する。この生成熱は懐炉などの熱源とし
て用いることができる。
The details of the present invention will be explained below. When the metal is M and C o H n is R, for example, when carboxylic acid is used as a reaction aid, the following reaction formula
As shown in (1), (2), and (3), the oxidation reaction progresses and generates heat of formation. This generated heat can be used as a heat source for hand warmers and the like.

M+XRCOOH→M(RCOO)x+H2 ……(1) M(RCOO)x+XH2O→M(OH)x+RCOOH
……(2) M(OH)x+YO2→MxOy+XH2O ……(3) 上記反応式からも明らかなようにカルボン酸は
未反応の金属がなくなるまで順次反応助成物とし
て働く。これらの有機酸は自然界においては微生
物によつて分解されるものであり、したがつて自
然破壊に対する破慮は必要でなく、また低コスト
で製造が可能であるなど優れた特長を有する。
M+XRCOOH→M(RCOO) x +H 2 ...(1) M(RCOO) x +XH 2 O→M(OH) x +RCOOH
...(2) M(OH) x + YO 2 →M x O y + . These organic acids are decomposed by microorganisms in nature, so there is no need to take precautions against natural destruction, and they have excellent features such as being able to be produced at low cost.

また上記発熱組成物を壊炉の発熱組成物として
利用した場合には、図面に示すように、適温(45
℃〜65℃)の得られる発熱時間が約20時間という
具合に、従来の発熱組成物Cに比較して約40%性
能が向上する。
In addition, when the above exothermic composition is used as a exothermic composition for a broken furnace, as shown in the drawing, it can be heated to an appropriate temperature (45
The exothermic time obtained (from 65°C to 65°C) is approximately 20 hours, which is an approximately 40% improvement in performance compared to the conventional exothermic composition C.

なお、反応助成物として用いる水溶性有機酸と
しては、蟻酸、酢酸、ハロゲン化酢酸、シユウ
酸、クエン酸および酒石酸などが有効である。特
にこの中でも酢酸およびクロル酢酸が好ましい。
またこれらの添加量は金属100重量部に対して0.5
重量部以上で反応助成効果は十分である。
Note that effective examples of water-soluble organic acids used as reaction aids include formic acid, acetic acid, halogenated acetic acid, oxalic acid, citric acid, and tartaric acid. Among these, acetic acid and chloroacetic acid are particularly preferred.
The amount of these additives is 0.5 per 100 parts by weight of metal.
The reaction promoting effect is sufficient at parts by weight or more.

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、その添加量は金属100重量部に対して
10〜100重量部、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
などの添加量は金属100重量部に対して10〜100重
量部が最適である。
In addition, water that is commonly used may be used, and the amount added is based on 100 parts by weight of metal.
The optimal amount of addition of raw ash, carbon such as activated carbon, silica gel, wood powder, etc. as a water retaining material that can impregnate water is 10 to 100 parts by weight per 100 parts by weight of metal.

さらに酸素としては空気を用いるのが一般的で
あるが、酸素ガス単体、あるいは化学反応により
発生する酸素を用いてもよい。
Further, although air is generally used as oxygen, oxygen gas alone or oxygen generated by a chemical reaction may also be used.

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。
Next, an example in which the exothermic composition of the present invention is applied as a hand warmer will be described.

発熱主成分として鉄粉30g、保水材としての素
灰10g、水15c.c.、水溶性有機酸として酢酸あるい
はモノクロル酢酸1gをよく混合し、この混合物
を、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120×85mmの袋内に
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(温度−発熱時間曲
線)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。
Thoroughly mix 30 g of iron powder as the main heating component, 10 g of raw ash as a water-retaining material, 15 cc. of water, and 1 g of acetic acid or monochloroacetic acid as a water-soluble organic acid. It was placed in a bag laminated with a sheet and having a size of 120 x 85 mm, and the opening of the bag was sealed by heat sealing, and the heat generation characteristics (temperature-heat generation time curve) as a hand warmer were measured. In this case, the heat generation temperature was measured using a copper constantan thermocouple at a temperature of 25°C and a humidity of 45°C.
It was carried out in a constant temperature and humidity room at %RH.

なお、従来品の反応助成物としては塩化銅を用
い、その添加量は最も特性が優れた結果を示す
1.5gを用い、かつその他の組成物の添加量は本
発明の実施例における有機酸を除いた他の組成物
と同様の組成比で行なつた。
In addition, copper chloride is used as a reaction aid in conventional products, and the amount of addition shows the results with the best characteristics.
1.5 g was used, and the amounts of other components added were the same as in the composition ratios of the other compositions in the Examples of the present invention except for the organic acid.

上記従来品と本発明の実施例品との測定結果は
図面に示す通りで、この図面からも明らかなよう
に、本発明の実施例品A(酢酸)、B(クロル酢酸)
は従来品Cに比べて適温の得られる発熱時間を著
しく長くすることができる。
The measurement results of the above conventional product and the example product of the present invention are as shown in the drawing, and as is clear from this drawing, the example products A (acetic acid) and B (chloroacetic acid) of the present invention.
Compared to conventional product C, it is possible to significantly lengthen the heat generation time at which an appropriate temperature can be obtained.

なお、上記実施例においては、水素よりもイオ
ン化傾向が大なる金属として鉄をあげたが、この
鉄に限定されるものではなく、アルミニウム、亜
鉛、マグネシウム等でも上記実施例と同様の作用
効果を発揮し得るものである。
In the above examples, iron was cited as a metal with a greater ionization tendency than hydrogen, but the metal is not limited to iron, and aluminum, zinc, magnesium, etc. can also have the same effect as in the above examples. It is something that can be demonstrated.

以上のように本発明の発熱組成物は、水素より
もイオン化傾向が大なる金属に、反応助成物とし
て水溶性有機酸を添加したものを有効成分とし、
水および酸素と反応して発熱するもので、反応助
成物として水溶性有機酸を用いているため、自然
破壊などの危険が少なく、かつ適温の得られる発
熱時間も例えば懐炉に使用した場合等従来品に比
較して著しく長くすることができるという優れた
特長を有する。
As described above, the exothermic composition of the present invention uses as an active ingredient a metal having a greater ionization tendency than hydrogen and a water-soluble organic acid added as a reaction aid,
It generates heat when it reacts with water and oxygen, and uses a water-soluble organic acid as a reaction aid, so there is less risk of natural destruction, and the heat generation time to maintain the appropriate temperature is longer than that of conventional methods, such as when used in a pocket warmer. It has the excellent feature that it can be made significantly longer than other products.

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

図は本発明の実施例品と従来品の発熱特性の比
較を示すグラフである。
The figure is a graph showing a comparison of heat generation characteristics between an example product of the present invention and a conventional product.

Claims (1)

【特許請求の範囲】[Claims] 1 水素よりもイオン化傾向が大なる金属に、反
応助成物として酢酸又はクロル酢酸からなる水溶
性有機酸を添加したものを有効成分とし、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。
1. An exothermic product characterized by the fact that the active ingredient is a metal that has a greater ionization tendency than hydrogen and a water-soluble organic acid such as acetic acid or chloroacetic acid is added as a reaction aid, and that it reacts with water and oxygen to generate heat. Composition.
JP7611379A 1979-06-15 1979-06-15 Exothermic composition Granted JPS561148A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP7611379A JPS561148A (en) 1979-06-15 1979-06-15 Exothermic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7611379A JPS561148A (en) 1979-06-15 1979-06-15 Exothermic composition

Publications (2)

Publication Number Publication Date
JPS561148A JPS561148A (en) 1981-01-08
JPS6324030B2 true JPS6324030B2 (en) 1988-05-19

Family

ID=13595835

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7611379A Granted JPS561148A (en) 1979-06-15 1979-06-15 Exothermic composition

Country Status (1)

Country Link
JP (1) JPS561148A (en)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5476120A (en) * 1977-11-29 1979-06-18 Fujitsu Ltd Electrical azimuth adjusting method in magnetic tape apparatus
JPS5476119A (en) * 1977-11-29 1979-06-18 Sony Corp Winding method of magnetic head

Also Published As

Publication number Publication date
JPS561148A (en) 1981-01-08

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