JPH0317874B2 - - Google Patents
Info
- Publication number
- JPH0317874B2 JPH0317874B2 JP1419882A JP1419882A JPH0317874B2 JP H0317874 B2 JPH0317874 B2 JP H0317874B2 JP 1419882 A JP1419882 A JP 1419882A JP 1419882 A JP1419882 A JP 1419882A JP H0317874 B2 JPH0317874 B2 JP H0317874B2
- Authority
- JP
- Japan
- Prior art keywords
- packaging material
- composition
- heat
- water
- air
- 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 - Lifetime
Links
- 239000000203 mixture Substances 0.000 claims description 64
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 44
- 239000005022 packaging material Substances 0.000 claims description 37
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 32
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 26
- 229910052742 iron Inorganic materials 0.000 claims description 20
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- 229910001868 water Inorganic materials 0.000 claims description 19
- 238000004519 manufacturing process Methods 0.000 claims description 18
- 239000011780 sodium chloride Substances 0.000 claims description 16
- 239000000945 filler Substances 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- -1 polypropylene Polymers 0.000 description 11
- 239000004698 Polyethylene Substances 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
- 229910001873 dinitrogen Inorganic materials 0.000 description 7
- 230000035699 permeability Effects 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000002245 particle Substances 0.000 description 4
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 3
- 229910001018 Cast iron Inorganic materials 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000020169 heat generation Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000004677 Nylon Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000004744 fabric Substances 0.000 description 2
- 235000013312 flour Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 229920001778 nylon Polymers 0.000 description 2
- 229920002239 polyacrylonitrile Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 235000019795 sodium metasilicate Nutrition 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 238000011056 performance test Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
- NASFKTWZWDYFER-UHFFFAOYSA-N sodium;hydrate Chemical class O.[Na] NASFKTWZWDYFER-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Thermotherapy And Cooling Therapy Devices (AREA)
Description
【発明の詳細な説明】
本発明は空気中の酸素と接触することによつて
発熱する発熱組成物の製造方法に関するものであ
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing an exothermic composition that generates heat upon contact with oxygen in the air.
即ち、金属鉄、塩化ナトリウム、活性炭、水お
よび充てん剤よりなる発熱組成物の製造におい
て、あらかじめ調製した塩化ナトリウム、活性
炭、水および充てん剤の混合物と金属鉄を夫々一
定量個々に、通気性を有する包装材料に充てん
し、ついでこれを気密性の包装材料に封入するこ
とを特徴とする発熱組成物の製造方法に関するも
のである。 That is, in the production of a heat-generating composition consisting of metallic iron, sodium chloride, activated carbon, water, and a filler, a pre-prepared mixture of sodium chloride, activated carbon, water, and a filler and a certain amount of metallic iron are individually mixed to improve air permeability. The present invention relates to a method for producing a heat-generating composition, characterized in that the heat-generating composition is filled into a packaging material containing the heat-generating composition, and then encapsulated in an airtight packaging material.
従来、金属鉄の化学反応による発熱組成物の製
造方法は、大別すると次の2つの方法がある。す
なわち(1)金属鉄、塩化ナトリウム、活性炭、水お
よび充てん剤の各成分を均一に混合調製して通気
性を有する包装材料に充てんし、ついでこれを気
密性の包装材料に封入する方法。(2)金属鉄、塩化
ナトリウム、活性炭、水および充てん剤の各成分
の内、金属鉄と水を含む組成物とを通気性を有す
る包装材料に分離して充てんし、ついでこれを気
密性の包装材料に封入する方法。これらのうち(1)
は金属鉄、塩化ナトリウム、活性炭、水および充
てん剤の各成分を均一に混合した組成物をあらか
じめ製造する。この組成物は空気と接触すると直
ちに発熱する。従つて組成物の製造から通気性を
有する包装材料に充てんするまで空気と接触しな
いようにする必要がある。その為、通常、空気を
窒素ガスと置換した密閉装置内で組成物を製造
し、さらに包装材料に充てんするまでの装置内も
空気を窒素ガスで置換することが行なわれてい
る。この為に装置が複雑となり、装置の製造費も
高価となる欠点がある。さらに製造時に大量の窒
素ガスを使用する為、その費用を必要とするとと
もに、窒素ガスが作業環境中に流出しないための
排気設備も必要となる。 Conventionally, methods for producing exothermic compositions by chemical reactions of metallic iron can be broadly classified into the following two methods. Namely, (1) a method in which each component of metallic iron, sodium chloride, activated carbon, water, and a filler is uniformly mixed and prepared, filled into a breathable packaging material, and then sealed in an airtight packaging material. (2) A composition containing metal iron and water among the components of metal iron, sodium chloride, activated carbon, water, and a filler is separated and filled into an air-permeable packaging material, and then this is airtight. Method of enclosing in packaging material. Of these (1)
A composition is prepared in advance by uniformly mixing each component of metallic iron, sodium chloride, activated carbon, water, and a filler. This composition generates heat immediately upon contact with air. Therefore, it is necessary to prevent the composition from coming into contact with air from the time the composition is manufactured until it is filled into a breathable packaging material. For this reason, the composition is usually manufactured in a closed device in which the air is replaced with nitrogen gas, and the air in the device is also replaced with nitrogen gas until the packaging material is filled. This has the disadvantage that the device becomes complicated and the manufacturing cost of the device is also high. Furthermore, since a large amount of nitrogen gas is used during manufacturing, it is expensive and requires exhaust equipment to prevent nitrogen gas from leaking into the working environment.
(2)の方法はすべての成分が混合されておらず、
特に金属鉄と水が分離されているため空気と接触
しても発熱することはないが、通気性を有する包
装材料に分離して充てんするため、通気性を有す
る包装材料の構造が複雑となる欠点がある。即
ち、製造時に、包装材料の1袋に2つの分離した
袋部分を設けると同時に各々に計量したものを充
てんしなければならない。さらに、分離した2つ
の袋の分離部分は容易に取りのぞけて一つの袋と
なるものでなければならない。この方法は(1)の方
法のように製造時に、空気と接触することを避け
る工夫は不必要であるが、包装材料が複雑となる
欠点がある。 In method (2), all the ingredients are not mixed,
In particular, since the metal iron and water are separated, they do not generate heat when they come into contact with air, but since they are separated and filled into breathable packaging materials, the structure of the breathable packaging material becomes complicated. There are drawbacks. That is, during manufacturing, a single bag of packaging material must be provided with two separate bag sections, each of which must be simultaneously filled with a measured amount. Furthermore, the separated parts of the two separated bags must be easily removed to form one bag. Unlike method (1), this method does not require any measures to avoid contact with air during production, but it has the disadvantage that the packaging material becomes complicated.
又、この方法で製造した発熱組成物は、使用者
が使用時に、2つの袋の間の分離部分を除去し混
合する操作が必要であり、使用者にとつて簡便な
ものではない。 Furthermore, the heat-generating composition produced by this method requires the user to remove the separated portion between the two bags and mix the two bags before use, which is not convenient for the user.
本発明者は上記2つの製造方法の長所、短所を
解明し、より経済的で簡便な発熱組成物の製造方
法を研究した結果、本発明に到達した。 The present inventor has elucidated the advantages and disadvantages of the above two manufacturing methods, and has researched a more economical and simple method of manufacturing a heat-generating composition, and as a result, has arrived at the present invention.
本発明は特に、金属鉄、塩化ナトリウム、活性
炭、水および充てん剤よりなる発熱組成物の製造
において;
(a) あらかじめ調製した塩化ナトリウム、活性
炭、水および充てん剤の混合物;ならびに
(b) 金属鉄;
のそれぞれを一定量用意し、その両者を同時に通
気性を有する1室の包装材料にそれぞれ充てん
し;
次いで
前記包装材料を気密性包装材料に封入することを
特徴とする発熱組成物の製造方法を提供するもの
である。 The invention particularly relates to the production of exothermic compositions consisting of metallic iron, sodium chloride, activated carbon, water and fillers; (a) a pre-prepared mixture of sodium chloride, activated carbon, water and fillers; and (b) metallic iron. A method for producing a heat-generating composition, comprising: preparing a certain amount of each of the following, and simultaneously filling both of them into a single chamber of air-permeable packaging material; and then encapsulating the packaging material in an airtight packaging material. It provides:
本発明はあらかじめ金属鉄をのぞく他の成分の
均一な混合物を調製する。これは活性炭と充てん
剤の混合物に塩化ナトリウムおよび処方によつて
は充てん剤を水に溶かした液を散布又は噴霧して
さらに混合することにより容易に製造できる。こ
の混合物は空気と接触しても発熱しないので、何
等、窒素ガス置換等の設備、操作を必要としな
い。従つてこの混合物は大量に製造して、水分が
減少しないようにプラスチツク製袋に入れて保存
することも可能である。製造時には、この混合物
と金属鉄を夫々個々に一定量計量しながら、その
両者を同時に通気性を有する1室の包装材料に充
てんする。ついでこの充てん物を気密性の包装材
料に封入して発熱組成物を得る。さらに、これら
の充てんの際、活性炭、塩化ナトリウム、水およ
び充てん剤の混合物と金属鉄の混合ができるよう
に、例えば包装材料への投入途中に障害物を設け
て衝突させて混合するなど、充てん装置を工夫す
ることもできる。又、本発明の製造方法では、混
合物と金属鉄が混合されるのは、通気性を有する
包装材料に充てんされると同時であり、充てん
後、気密性の包装材料に封入されるまでの時間も
短時間である。従つてその間は空気との接触もあ
るが、発熱が起ることなく製造できる。 In the present invention, a homogeneous mixture of other components except metallic iron is prepared in advance. This can be easily produced by sprinkling or spraying a mixture of activated carbon and filler with sodium chloride and, depending on the formulation, a solution of the filler dissolved in water. Since this mixture does not generate heat even when it comes into contact with air, it does not require any equipment or operations such as nitrogen gas replacement. This mixture can therefore be prepared in large quantities and stored in plastic bags to prevent loss of moisture. During manufacturing, the mixture and metal iron are individually weighed in predetermined amounts, and both are simultaneously filled into a single chamber of air-permeable packaging material. This filled material is then encapsulated in an airtight packaging material to obtain a heat generating composition. Furthermore, when filling these materials, in order to mix the mixture of activated carbon, sodium chloride, water, and filler with metal iron, for example, an obstacle is set up on the way to the packaging material so that they collide and mix. The device can also be devised. Furthermore, in the manufacturing method of the present invention, the mixture and metal iron are mixed at the same time as they are filled into the air-permeable packaging material, and the time from filling until the mixture is sealed in the air-tight packaging material is shortened. is also short-lived. Therefore, although there is some contact with air during this period, production can be performed without generating heat.
先に説明の従来の方法では、窒素ガス置換を行
つていても発熱組成物を供給するホツパー容器等
が手で触れない程の高温となる。この事は、本来
の発熱組成物が有する発熱性能が維持されず、製
造時の発熱による損失が大きいと考えられる。一
方、本発明は以上詳述の如く損失が全くなく、本
来の性能を持つ発熱組成物が得られる。 In the conventional method described above, even when nitrogen gas replacement is performed, the hopper container and the like that supply the exothermic composition reach a high temperature that cannot be touched by hand. This is considered to be due to the fact that the original heat generating performance of the heat generating composition is not maintained and there is a large loss due to heat generation during production. On the other hand, according to the present invention, as detailed above, there is no loss and a heat generating composition having the original performance can be obtained.
さらに従来の方法(1)では、発熱の損失ととも
に、その発熱済の組成物が固りとなつて組成物に
混在する。これら発熱組成物は本来人間のからだ
に付けて保温の目的に使用するものであるから、
固りが混在すると違和感もしくは痛みを感じるこ
とがあり好ましくない。本発明の製造方法によれ
ば、固りは全くなく、からだに付けた際にも柔ら
かいすぐれた発熱組成物が得られる。 Furthermore, in the conventional method (1), as well as the loss of heat generation, the heated composition becomes a solid and is mixed in the composition. These exothermic compositions are originally used for the purpose of keeping people warm by applying them to the human body.
Mixing stiffness may cause discomfort or pain, which is not desirable. According to the manufacturing method of the present invention, an excellent heat-generating composition that is completely free of hardness and soft even when applied to the body can be obtained.
発熱組成物と同じような反応系を示すものとし
て酸素吸収剤があるが、この場合はその反応がゆ
るやかで、発熱を伴なわず、その利用面において
も有効期間は長時間にわたるものである。一方、
本発明の発熱組成物の場合は、反応が短時間に急
激に行われるものであり、原理には共通点が多々
見られるものの、細部にわたつては両者は非常に
異つている。例えば、酸素吸収剤の場合、全ての
原料を窒素ガスのごとき不活性ガスの存在下で製
造する必要はない。本発明において、あらかじめ
金属鉄に塩化ナトリウムを被覆したものを使うと
発熱温度は低下し、保存中に発熱特性の劣化が見
られ、発熱組成物としての特長を失う。従つて、
本発明のごとく塩化ナトリウムは金属鉄以外のも
のとあらかじめ調製する必要がある。 Oxygen absorbers exhibit a reaction system similar to that of exothermic compositions, but in this case, the reaction is slow and does not generate heat, and their useful life is long. on the other hand,
In the case of the exothermic composition of the present invention, the reaction occurs rapidly in a short period of time, and although there are many similarities in principle, the two are very different in detail. For example, in the case of oxygen absorbers, it is not necessary to produce all raw materials in the presence of an inert gas such as nitrogen gas. In the present invention, if metal iron coated with sodium chloride in advance is used, the exothermic temperature will be lowered, the exothermic properties will deteriorate during storage, and the composition will lose its characteristics as an exothermic composition. Therefore,
As in the present invention, sodium chloride must be prepared in advance with something other than metal iron.
本発明において製造する発熱組成物は、金属鉄
を主成分として含むものであるが、この金属鉄と
しては還元粉、電解粉、噴霧粉、樢砕粉などの粉
末状のものが使用できる。一般に50メツシユより
小さい平均粒子径のものが適当であり、必らずし
も高純度のものでなくても本発明の効果を損なわ
れない程度で不純物を含有していてもよく、好ま
しい例としては鋳鉄粉があげられる。又、本発明
の組成物に使用する充てん剤としては、保存中の
品質、性能が維持でき、一定温度の発熱が長時間
得られ、その間もんだり、振つたりする必要をな
くするためケイ酸ナトリウム含水塩が使用され
る。又、充てん剤として、ケイソウ土、木粉、素
灰、硫酸カルシウム、酸性白土、ゼオライト等が
使用でき、これらのものを使用することによつ
て、発熱組成物の流動性、柔軟性が向上し、から
だに付けた時の感じをよくし、又スムーズな発熱
が得られる。その他水を吸収させてそれを安定に
保持させる目的で吸水性高分子を使用することも
できる。吸水性高分子を使用すると発熱組成物に
圧力がかかつても水を分離することなく、安定に
保持させることが可能であり、発熱組成物の反応
には全く影響がない。この吸水性高分子として
は、CMC系、デンプン−ポリアクリロニトリル
加水分解物、デンプン−ポリアクリル酸塩架橋
物、酢酸ビニル−アクリル酸メチル共重合体ケン
化物、ポリアクリロニトリル加水分解物、ポリア
クリル酸ナトリウム架橋物などが使用できる。 The heat-generating composition produced in the present invention contains metallic iron as a main component, and this metallic iron can be in powder form such as reduced powder, electrolytic powder, spray powder, or crushed oak powder. In general, particles with an average particle size smaller than 50 mesh are suitable, and even if they are not necessarily highly pure, they may contain impurities to the extent that they do not impair the effects of the present invention. can include cast iron powder. In addition, as a filler used in the composition of the present invention, silicic acid is used because it can maintain quality and performance during storage, generate heat at a constant temperature for a long time, and eliminate the need for kneading or shaking during that time. Sodium hydrate salts are used. In addition, diatomaceous earth, wood flour, raw ash, calcium sulfate, acid clay, zeolite, etc. can be used as fillers, and by using these materials, the fluidity and flexibility of the exothermic composition are improved. , it feels good when you put it on your body, and it generates heat smoothly. In addition, water-absorbing polymers can also be used for the purpose of absorbing water and stably retaining it. When a water-absorbing polymer is used, even if pressure is applied to the exothermic composition, water can be stably retained without separating, and the reaction of the exothermic composition is not affected at all. Examples of this water-absorbing polymer include CMC type, starch-polyacrylonitrile hydrolyzate, starch-polyacrylate crosslinked product, saponified vinyl acetate-methyl acrylate copolymer, polyacrylonitrile hydrolyzate, and sodium polyacrylate. Cross-linked materials etc. can be used.
本発明の発熱組成物は前述のごとく、通気性を
有する包装材料に充てんされる。この包装材料は
酸素と組成物の接触を制御し、また組成物が外部
へ漏出するのを防止する。従つてこの包装材料と
しては組成物の混合物が外部にでず、空気(酸
素)が適度に通るものであることが必要である。
この包装材料は発熱組成物を充てん包装すると
き、全体が均一な空気通気性を有するものが望ま
しい。通気性が部分的に異なつていたり、局部的
に通気性を有するような包装材料は適当でない。
例えば、全体に均一にあけられた小さな穴を有す
る紙、合成紙又はナイロン、ポリエステルなどの
不織布、又は穴をあけたフイルムを紙、合成紙、
又は不織布に積層したものが好ましい。 As described above, the heat-generating composition of the present invention is filled into a breathable packaging material. This packaging material controls the contact of the composition with oxygen and also prevents the composition from leaking out. Therefore, the packaging material needs to be one that does not allow the mixture of the composition to escape to the outside and allows a suitable amount of air (oxygen) to pass through.
This packaging material desirably has uniform air permeability throughout when the heat-generating composition is filled and packaged. Packaging materials that differ in their air permeability or have local air permeability are not suitable.
For example, paper, synthetic paper, or non-woven fabric such as nylon or polyester, or a film with holes made in it, can be used as paper, synthetic paper, or
Alternatively, one laminated on a nonwoven fabric is preferable.
又、発熱組成物を充てんした包装材料を封入す
る気密性を有する包装材料としてはOV−ポリエ
チレンあるいは塩化ビニリデンを被覆したポリプ
ロピレン、ポリエステル等のフイルムとポリエチ
レンを積層した気密性のフイルムで作つたものが
好ましい。 In addition, as an airtight packaging material for enclosing a packaging material filled with a heat-generating composition, one made of an airtight film laminated with a film of OV-polyethylene or polypropylene coated with vinylidene chloride, polyester, etc., and polyethylene. preferable.
次に実施例で本発明を説明する。 Next, the present invention will be explained with examples.
但し実施例中「部」とあるのは「重量部」を示
す。 However, "parts" in the examples indicate "parts by weight."
実施例 1
塩化ナトリウム6部とメタケイ酸ナトリウム9
水塩6部を水48部にけん濁した液を、ケイソウ土
28部と活性炭12部の混合物に含浸させた。この混
合物30gと平均粒度80メツシユの鋳鉄粉30gを
夫々、ガーレー式デンソメーターでの測定値が、
15〜20秒/100mlの通気性を有するナイロンスパ
ンボンド−ポリエチレンよりなる10×13cmの包装
材料に同時に充てんした。ついで塩化ビニリデン
コートポリプロピレン50μ−ポリエチレン40μの
フイルムよりなる気密性の包装材料(13×17cm)
に封入して発熱組成物を得た。Example 1 6 parts of sodium chloride and 9 parts of sodium metasilicate
A suspension of 6 parts of aqueous salt in 48 parts of water is made from diatomaceous earth.
It was impregnated with a mixture of 28 parts and 12 parts of activated carbon. The measured values of 30 g of this mixture and 30 g of cast iron powder with an average particle size of 80 mesh using a Gurley densometer were as follows.
A 10 x 13 cm packaging material made of nylon spunbond polyethylene with an air permeability of 15-20 seconds/100 ml was simultaneously filled. Next, an airtight packaging material (13 x 17 cm) made of vinylidene chloride coated polypropylene 50μ - polyethylene 40μ film.
A heat-generating composition was obtained.
実施例 2
塩化ナトリウム7部とメタケイ酸ナトリウム9
水塩7部を水47部にけん濁した液を、活性炭14
部、木粉23部および酢酸ビニル−アクリル酸メチ
ル共重合体ケン化物2部の混合物に噴霧して含浸
させ、さらに混合して均一な混合物を得た。この
混合物25gと、平均粒度100メツシユの鋳鉄粉35
gを夫夫同時にガーレー式デンソメーターによる
測定値が18〜23秒/100mlのパルプと合成樹脂よ
りなる合成紙−ポリエチレン製割布−ポリエチレ
ンの三層よりなる通気性を有する包装材料に充て
んし、9.5×14cmの充てん物を得た。ついでOV−
ポリエチレンのフイルムよりなる12.5×17.5cmの
気密性を有する包装材料の袋に封入して発熱組成
物を得た。Example 2 7 parts of sodium chloride and 9 parts of sodium metasilicate
A solution prepared by suspending 7 parts of water salt in 47 parts of water was added to 14
1 part, 23 parts of wood flour, and 2 parts of saponified vinyl acetate-methyl acrylate copolymer. 25 g of this mixture and 35 g of cast iron powder with an average particle size of 100 mesh
The husband and husband simultaneously filled the air-permeable packaging material made of three layers: synthetic paper made of pulp and synthetic resin, polyethylene cloth, and polyethylene, with a value measured by a Gurley densometer of 18 to 23 seconds per 100 ml. A filling of 9.5×14 cm was obtained. Then OV-
A heat-generating composition was obtained by sealing it in a 12.5 x 17.5 cm airtight packaging material bag made of polyethylene film.
実施例 3
塩化ナトリウム9部を水27部に溶解し、ケイソ
ウ土54部と活性炭10部の混合物に散布して含浸さ
せた。この混合物40gと還元鉄粉(RD−3.日本
鉄粉製)20gを同時に、ガーレー式デンソメータ
ー測定値8〜12秒/100mlの通気性を有するレー
ヨン紙−ポリエチレン製割布−ポリエチレンの三
層よりなる包装材料(10×13.5cm)に充てんし
た。ついでこれを塩化ビニリデンコートポリエス
テル15μ−ポリエチレン60μのフイルムよりなる
気密性の包装材料(13×17cm)に封入して発熱組
成物を得た。Example 3 9 parts of sodium chloride was dissolved in 27 parts of water and sprinkled on a mixture of 54 parts of diatomaceous earth and 10 parts of activated carbon to impregnate it. 40g of this mixture and 20g of reduced iron powder (RD-3. manufactured by Nippon Steel Powder) were simultaneously mixed into three layers of rayon paper, polyethylene cloth, and polyethylene, each having an air permeability of 8 to 12 seconds per 100ml measured using a Gurley densometer. The packaging material (10 x 13.5 cm) was filled with: This was then encapsulated in an airtight packaging material (13 x 17 cm) made of a film of vinylidene chloride coated polyester 15μ and polyethylene 60μ to obtain a heat generating composition.
性能試験
上記実施例1,2および3の本発明の製造方法
による発熱組成物を気密性の包装材料から取り出
し、室温20℃の部屋でタオル4枚につつみ、測温
抵抗体により温度を測定した。いずれの発熱組成
物も最高温度60〜70℃、40℃以上の持続時間が20
時間以上ですぐれた発熱性能を示した。Performance Test The exothermic composition produced by the production method of the present invention in Examples 1, 2, and 3 above was taken out from the airtight packaging material, wrapped in four towels in a room at a room temperature of 20°C, and the temperature was measured using a resistance thermometer. . Both exothermic compositions have a maximum temperature of 60 to 70℃, and a duration of 20 degrees above 40℃.
It showed excellent heat generation performance over hours.
Claims (1)
充てん剤よりなる発熱組成物の製造において; (a) あらかじめ調製した塩化ナトリウム、活性
炭、水および充てん剤の混合物;ならびに (b) 金属鉄; のそれぞれを一定量用意し、その両者を同時に通
気性を有する1室の包装材料に充てんし; 次いで 前記包装材料を気密性包装材料に封入することを
特徴とする発熱組成物の製造方法。[Claims] 1. In the production of an exothermic composition comprising metallic iron, sodium chloride, activated carbon, water and a filler; (a) a previously prepared mixture of sodium chloride, activated carbon, water and a filler; and (b) Preparing a certain amount of each of metal iron; and filling both of them simultaneously into a single chamber of air-permeable packaging material; and then encapsulating the packaging material in an airtight packaging material. Method.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57014198A JPS58132074A (en) | 1982-01-29 | 1982-01-29 | Preparation of pyrogenic composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57014198A JPS58132074A (en) | 1982-01-29 | 1982-01-29 | Preparation of pyrogenic composition |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1312136A Division JPH0368680A (en) | 1989-11-30 | 1989-11-30 | Manufacture of heat generating composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS58132074A JPS58132074A (en) | 1983-08-06 |
JPH0317874B2 true JPH0317874B2 (en) | 1991-03-11 |
Family
ID=11854417
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57014198A Granted JPS58132074A (en) | 1982-01-29 | 1982-01-29 | Preparation of pyrogenic composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58132074A (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0759839B2 (en) * | 1990-07-07 | 1995-06-28 | 戸田建設株式会社 | Reinforcing bar joint method |
US6099556A (en) * | 1995-05-27 | 2000-08-08 | Kabushiki Kaisha Genchi Kenkyusho | Method of controlling exothermic reaction of an exothermic composition, the exothermic composition, an exothermic device and an application pad |
AU6173796A (en) * | 1995-06-29 | 1997-01-30 | Procter & Gamble Company, The | Thermal neck wrap having wing shape and means for position maintenance |
ATE245009T1 (en) * | 1995-06-29 | 2003-08-15 | Procter & Gamble | ELASTIC BACK HEATING BELT WITH A DIAMOND-SHAPED HEAT PAD AND ANTI-SLIP AGENTS |
JP4547046B2 (en) * | 1995-06-29 | 2010-09-22 | ワイス・エルエルシー | Heat cell |
US5728058A (en) * | 1995-06-29 | 1998-03-17 | The Procter & Gamble Company | Elastic knee wrap |
US5984995A (en) * | 1996-03-29 | 1999-11-16 | The Procter & Gamble Company | Heat cells |
US20020020406A1 (en) | 1998-09-06 | 2002-02-21 | Naoki Minami | United exothermic medium and heating element using it |
-
1982
- 1982-01-29 JP JP57014198A patent/JPS58132074A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS58132074A (en) | 1983-08-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2620815C (en) | Heat cells comprising exothermic compositions having absorbent gelling material | |
KR100303200B1 (en) | Heat cells | |
AU2006293469B2 (en) | A method of making heat cells comprising exothermic compositions having absorbent gelling material | |
JPS5835706B2 (en) | A chemical pot that generates heat by adding water during use. | |
JPH0420657B2 (en) | ||
KR0130460B1 (en) | Oxygen absorber and method for producing same | |
CN107614422A (en) | Chlorine dioxide generator and its manufacture method | |
JPH0317874B2 (en) | ||
JP4018284B2 (en) | Composition containing inorganic porous crystal-hydrophilic polymer composite and molded product thereof | |
SK87699A3 (en) | A thermal pack having a plurality of individual heat cells | |
JP3648323B2 (en) | Method for producing iron-based oxygen absorbent | |
JP3252866B2 (en) | Oxygen absorber | |
JPH0353349B2 (en) | ||
JP7055957B1 (en) | Manufacturing method of heating element and heating element | |
JP3187305B2 (en) | Oxygen scavenger and water donating carrier for oxygen scavenger | |
JPH04293989A (en) | Manufacture of heat generating composition | |
JPS59229131A (en) | Exothermic object to be used in chemical pocket warmer served by adding water when in use | |
JPH01202281A (en) | Deoxidation agent for culture of anaerobic bacteria | |
JPH10323531A (en) | Desiccant and its production | |
JPH03202150A (en) | Preparation of oxygen absorbent | |
JPS58128145A (en) | Oxygen absorbing agent | |
JPS5884039A (en) | Material for packing absorbent of gaseous carbonic acid | |
JP2600901B2 (en) | Manufacturing method of oxygen absorber | |
JP2005073895A (en) | Heat insulating package | |
JPH02298344A (en) | Manufacture of oxygen absorbent |