JPS6114283A - Thermal energy storage material composition - Google Patents

Thermal energy storage material composition

Info

Publication number
JPS6114283A
JPS6114283A JP59135879A JP13587984A JPS6114283A JP S6114283 A JPS6114283 A JP S6114283A JP 59135879 A JP59135879 A JP 59135879A JP 13587984 A JP13587984 A JP 13587984A JP S6114283 A JPS6114283 A JP S6114283A
Authority
JP
Japan
Prior art keywords
latent heat
energy storage
temperature phase
thermal energy
compsn
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.)
Pending
Application number
JP59135879A
Other languages
Japanese (ja)
Inventor
Mitsuo Masushige
増茂 光男
Nobuhiro Kudou
工藤 順啓
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.)
Adeka Corp
Original Assignee
Asahi Denka Kogyo KK
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 Asahi Denka Kogyo KK filed Critical Asahi Denka Kogyo KK
Priority to JP59135879A priority Critical patent/JPS6114283A/en
Publication of JPS6114283A publication Critical patent/JPS6114283A/en
Pending legal-status Critical Current

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/14Thermal energy storage

Abstract

PURPOSE:To provide a thermal energy storage material compsn. which can be repeatedly used and dissipates heat only when required, containing a salt hydrate which can be supercooled and emits latent heat in the transition from a high- temperature phase to a low-temperature phase, and a hydroxylpropylated guar gum. CONSTITUTION:The titled thermal energy storage material contains a salt hydrate (A) (e.g. calcium chloride hexahydrate or sodium carbonate decahydrate) which can be supercooled and emits latent heat in the transition from a high- temperature phase to a low-temperature phase, and 0.2-1.5wt% (based on the quantity of compsn.) hydroxypropylated guar gum (B) as essential ingredients. The compsn. accumulates latent heat by heating and retains the latent heat in a supercooling state at room temp. When required, a seed crystal is added thereto, or a stimulus is given to the compsn. by a sharp metal stick to thereby break supercooling, whereby latent heat is dissipated. In this way, the heating and the breaking of supercooling are repeatedly made, whereby thermal energy storage and heat dissipation can be repeated.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明はM熱剤組成物に関するものである。[Detailed description of the invention] [Industrial application field] The present invention relates to an M heating agent composition.

特に本発明は、加熱により蓄積された潜熱を過冷却状態
で保持し必要な時に過冷却を破壊して蓄積されている潜
熱を取り出すことができる、繰り返し使用可能な蓄熱剤
組成物に関するものである。
In particular, the present invention relates to a reusable heat storage agent composition that can retain latent heat accumulated through heating in a supercooled state and, when necessary, destroy the supercooling and extract the accumulated latent heat. .

〔従来の技術〕[Conventional technology]

太陽エネルギー等の蓄熱のために潜熱蓄熱剤が種々開発
されているが、その殆どは過冷却を防止した系で使用さ
れている。もっとも、過冷却を利用した蓄熱剤自体は公
知であり、例えば米国特許第4.077.390号明細
書には酢酸ナトリウム3水和物を使用した蓄熱パンクが
記載されている。又、特開昭59−53578号公報に
は酢酸ナトリウム3水和物とキサンタンガムを含有する
蓄熱体が記載されている。
Various latent heat storage agents have been developed for storing heat such as solar energy, but most of them are used in systems that prevent supercooling. However, heat storage agents that utilize supercooling are known per se; for example, US Pat. No. 4,077,390 describes a heat storage puncture using sodium acetate trihydrate. Further, JP-A-59-53578 describes a heat storage body containing sodium acetate trihydrate and xanthan gum.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

米国特許第4.077.390号明細書に記載の如く、
酢酸ナトリウム3水和物の水溶液をそのまま使用する場
合は、容器の蓋等に付着する結晶が過冷却されている系
に振動等で落下したりして不必要な時に過冷却が破壊さ
れやす(、安定な系とは言えないという欠点を有するも
のである。
As described in U.S. Pat. No. 4,077,390,
When using an aqueous solution of sodium acetate trihydrate as is, crystals attached to the lid of the container may fall into the supercooled system due to vibrations, etc., and the supercooling may be destroyed at an unnecessary time ( However, it has the disadvantage that it cannot be said to be a stable system.

又、特開昭59−53578号公報に記載の組成物は、
上記の点を改良したものであるが、繰り返しの加熱放熱
によりガムと無機塩等が分離を起こし、ガム添加の効果
が減少してしまう欠点がある。
Furthermore, the composition described in JP-A No. 59-53578 is
Although this is an improvement on the above points, it has the disadvantage that the gum and inorganic salts, etc. separate due to repeated heating and heat radiation, reducing the effect of adding gum.

本発明の目的は必要な特進安定に過冷却が保護され、繰
り返し使用が可能な潜熱蓄熱剤を提供することにある。
An object of the present invention is to provide a latent heat storage agent that can protect against supercooling with the necessary special stability and can be used repeatedly.

(問題点を解決するための手段) 本発明のM熱剤組成物は、必須の構成成分として、過冷
却可能で、高温相から低温相に移転する際に潜熱を放出
する塩水和物と、ヒドロキシプロピル化グアーガムとを
含有するものである。
(Means for Solving the Problems) The M heat agent composition of the present invention includes, as an essential component, a salt hydrate that can be supercooled and releases latent heat when transferring from a high temperature phase to a low temperature phase; It contains hydroxypropylated guar gum.

以下、本発明の蓄熱剤組成物について詳述する。Hereinafter, the heat storage agent composition of the present invention will be explained in detail.

本発明に使用される過冷却可能で、高温相から低温相に
移転する際に潜熱を放出する塩水和物としては、例えば
塩化カルシウム6水和物(融点29℃)、炭酸ナトリウ
ム10水和物(融点35℃)、燐酸2ナトリウム12水
和物(融点35.5℃)、硝酸カルシウム4水和物(融
点42.7℃)、硫酸ナトリウム10水和物(融点32
℃)、チオ硫酸ナトリウム5水和物(融点50℃)、酢
酸ナトリウム3水和物(融点5°8℃)、水酸化バリウ
ム8水和物(融点35℃)、硝酸亜鉛6水和物(融点5
0℃)、フン化カリウム4水和。物(融点18.5℃)
等を使用することができ、用途に応じた融点の材料を選
択使用すればよい。これらの塩水和物は、本発明の蓄熱
剤組成物の主体を構成するもので、通常、組成物の90
重量%以上を占める。
Salt hydrates that can be supercooled and release latent heat when transferring from a high temperature phase to a low temperature phase used in the present invention include, for example, calcium chloride hexahydrate (melting point 29°C), sodium carbonate decahydrate (melting point 35°C), disodium phosphate decahydrate (melting point 35.5°C), calcium nitrate tetrahydrate (melting point 42.7°C), sodium sulfate decahydrate (melting point 32°C),
), sodium thiosulfate pentahydrate (melting point 50°C), sodium acetate trihydrate (melting point 5°8°C), barium hydroxide octahydrate (melting point 35°C), zinc nitrate hexahydrate ( Melting point 5
0°C), potassium fluoride tetrahydrate. (melting point 18.5℃)
etc., and it is sufficient to select and use a material with a melting point depending on the purpose. These salt hydrates constitute the main body of the heat storage agent composition of the present invention, and usually make up 90% of the composition.
It accounts for more than % by weight.

本発明に使用されるヒドロキシプロピル化グアーガムと
しては、例えば、二晶株式会社製商品名ジャガーHP等
があり、置換度が構成糖当り0.3〜0.6である商品
としては、ジャガーHP−8、ジャガーHP −1’ 
1及びジャガーHP−60かある。
Examples of the hydroxypropylated guar gum used in the present invention include Jaguar HP manufactured by Niksho Co., Ltd., and products with a substitution degree of 0.3 to 0.6 per constituent sugar include Jaguar HP- 8. Jaguar HP -1'
1 and Jaguar HP-60.

ヒドロキシプロピル化グアーガムの使用量は必要とされ
る蓄熱剤組成物の粘度等を考慮して決定すればよいが、
通常は組成物に対して0.2重量%〜1.5重量%程度
(粘度を50cp〜10000cp゛程度とする量)で
あり、好ましくは0.3重量%〜0.6重量%程度(粘
度を70cp〜500cp程度とする量)である。尚、
本発明の蓄熱剤組成物は、粘度を上記範囲、即ち、50
cp〜10000cp、好ましくは70cp〜500C
11に調整するのが過冷却状態を安定に保持する上から
好ましい。
The amount of hydroxypropylated guar gum to be used may be determined by considering the viscosity of the required heat storage agent composition, etc.
Usually, the amount is about 0.2% to 1.5% by weight (the amount that makes the viscosity about 50cp to 10,000cp), preferably about 0.3% to 0.6% by weight (viscosity of about 70 cp to 500 cp). still,
The heat storage agent composition of the present invention has a viscosity within the above range, that is, 50
cp~10000cp, preferably 70cp~500C
It is preferable to adjust the temperature to 11 from the viewpoint of stably maintaining the supercooled state.

また、本発−〇蓄熱剤組成物の、過冷却状態を    
     1一層安定に保持する上で、上記2つの必須
成分の他に、該組成物に融点80℃以下の多価アルコー
ル、例えば、プロピレングリコール、エチレングリコー
ル、グリセリン等を1〜5重量重量%台有させるのが好
ましく、更に必要に応じて水、殺菌剤、着色剤等を含有
させることができる。
In addition, the supercooled state of the heat storage agent composition of this invention
1. In addition to the above two essential components, the composition may contain 1 to 5% by weight of a polyhydric alcohol with a melting point of 80° C. or less, such as propylene glycol, ethylene glycol, glycerin, etc., in order to maintain the stability. It is preferable to add water, a disinfectant, a coloring agent, etc., if necessary.

本発明の蓄熱剤組成物は、その製法には特に限定される
ものではなく、例えば、後記の実施例に示す如き方法に
よって製造される。
The heat storage agent composition of the present invention is not particularly limited in its manufacturing method, and can be manufactured, for example, by a method as shown in Examples below.

〔作用〕[Effect]

本発明の蓄熱剤組成物は、室温では、加熱により蓄熱し
た潜熱を安定な過冷却状態で保持しており、過冷却状態
を破壊すれば潜熱を放出するもので、上記の加熱・過冷
却破壊を繰り返し行うことにより、上記の蓄熱・放熱作
用が繰り返して行われる。
At room temperature, the heat storage agent composition of the present invention retains the latent heat accumulated through heating in a stable supercooled state, and when the supercooled state is broken, the latent heat is released. By repeating this, the heat storage and heat dissipation effects described above are repeatedly performed.

〔実施例〕〔Example〕

以下に本発明の実施例を示すが、本発明はこれに限定さ
れるものではない。
Examples of the present invention are shown below, but the present invention is not limited thereto.

実施例1 冷却器及び温度針を付けた攪拌機付の300m1セパラ
ブルフラスコに蒸溜水19.4 gを加え、こを80℃
のウオターパス中に設置する。攪拌機を攪拌しながら上
記蒸溜水中にヒドロキシプロピル化グアーガム(商品名
[ジャガーHPJ三晶株式会社)1.2gを徐々に添加
し、だまを作らず均一に分散溶解させて粘性を有する溶
液を得た。次いで、この粘性溶液に120.6gの無水
酢酸ナトリウムを加え、この混合物を十分に攪拌しなが
ら80℃に加温し固形粒子が完全に溶解し、均一な透明
な粘稠溶液となるまで攪拌した。この際、水の損失を防
ぐため水冷却器を用いた。
Example 1 19.4 g of distilled water was added to a 300 ml separable flask equipped with a stirrer and a condenser and a temperature needle, and the mixture was heated to 80°C.
Installed in the water pass. While stirring with a stirrer, 1.2 g of hydroxypropylated guar gum (trade name: Jaguar HPJ Sansho Co., Ltd.) was gradually added to the distilled water, and the mixture was uniformly dispersed and dissolved without forming lumps to obtain a viscous solution. . Next, 120.6 g of anhydrous sodium acetate was added to this viscous solution, and the mixture was heated to 80° C. with sufficient stirring until the solid particles were completely dissolved and a homogeneous transparent viscous solution was obtained. . At this time, a water cooler was used to prevent water loss.

上記の透明な粘稠溶液を300m1のネジフタを有する
透明な肉厚ガラスビンに移し、このビンをゆっ(りと室
温まで冷却した。このようにして得た混合物(蓄熱剤組
成物)に酢酸ナトリウム3水和物の種結晶を入れるか又
は先のとがった金属棒で刺激を与えることにより上記混
合物の結晶化を誘発させた。その結果、上記混合物(蓄
熱剤組成物)は直ちにその潜熱を発散して55℃に上昇
した。
The above clear viscous solution was transferred to a 300 ml clear thick-walled glass bottle with a screw cap and the bottle was slowly cooled to room temperature. Crystallization of the mixture was induced by introducing hydrate seed crystals or by stimulating with a pointed metal rod.As a result, the mixture (heat storage agent composition) immediately released its latent heat. The temperature rose to 55°C.

上記混合物を、80℃に再び加熱して再び均一な透明な
粘稠溶液となるまで溶かし、再度室温まで徐冷した。こ
の混合物は、前記と同様に再び結晶化を誘発させること
が出来、潜熱を発散して55℃に上昇した。この操作を
60回繰り返したが全て同じ結果が得られた。
The above mixture was heated again to 80° C. until it became a homogeneous, transparent, viscous solution again, and then slowly cooled to room temperature again. This mixture was able to induce crystallization again as before, giving off latent heat and rising to 55°C. This operation was repeated 60 times, but the same result was obtained.

また、この混合物は60回同じ操作を繰り返しても、色
調は殆ど変わらず、80℃の粘稠溶液とした場合にヒド
ロキシプロピル化グアーガムの凝集、分離もなく、良好
な粘稠度を保持していた。
Furthermore, even after repeating the same operation 60 times, the color tone of this mixture hardly changed, and when it was made into a viscous solution at 80°C, there was no aggregation or separation of the hydroxypropylated guar gum, and it maintained a good consistency. Ta.

更に、この粘稠溶液を冷却させてから、室温で10.0
日間放置した後、この混合物に酢酸ナトリウム3水和物
の種結晶の種入れ又は先のとがった金属棒で刺戟を与え
ることにより混合物は急に温度が55℃に上昇した。次
いで、この混合物を再び80℃に加温し、再び透明なる
粘稠溶液として再び室温まで冷却した。この混合物に前
記と同様な刺戟を与えると前記と同様な結果が得られた
Further, this viscous solution was allowed to cool down and then 10.0
After standing for a day, the mixture was seeded with sodium acetate trihydrate seed crystals or stimulated with a pointed metal rod, causing the mixture to suddenly rise in temperature to 55°C. The mixture was then warmed again to 80° C. and cooled again to room temperature as a clear viscous solution. When this mixture was given the same stimulus as above, similar results were obtained.

実施例2 実施例1で用いた装置を用い、その300m1のフラス
コに、ヒドロキシプロピル化グアーガム1゜6gを入れ
、これにプロピレングリコール16gを添加し、該ヒド
ロキシプロピル化グアーガムを湿潤分散させ、攪拌しな
がら、蒸溜水79.4 gを加え、更に攪拌しながら8
0℃まで加温し、均一な透明な溶液とした後、これに無
水酢酸ナトリウム120.6gを加え、完全に熔解させ
均一な透明な粘稠溶液となるまで攪拌した。この際、水
の損失を防ぐため水冷却を用いた。
Example 2 Using the apparatus used in Example 1, 1.6 g of hydroxypropylated guar gum was placed in a 300 ml flask, 16 g of propylene glycol was added thereto, the hydroxypropylated guar gum was wet-dispersed, and the mixture was stirred. While stirring, add 79.4 g of distilled water, and add 79.4 g of distilled water while stirring.
After heating to 0° C. to form a uniform, transparent solution, 120.6 g of anhydrous sodium acetate was added thereto, and the mixture was stirred until completely melted to form a uniform, transparent, viscous solution. At this time, water cooling was used to prevent water loss.

上記の透明な粘稠溶液を実施例1と同様にネジフタ付肉
厚ガラスビンに移しゆっくり室温まで冷却した。このよ
うにして得た混合物(蓄熱剤組成物)に実施例1と同じ
操作で刺戟を与え、上記混合物の結晶化を誘発させた。
The above clear viscous solution was transferred to a thick-walled glass bottle with a screw cap in the same manner as in Example 1, and slowly cooled to room temperature. The mixture thus obtained (heat storage agent composition) was stimulated in the same manner as in Example 1 to induce crystallization of the mixture.

その結果、上記混合物(M処刑組成物)は直ちにその潜
熱を発散して55℃に上昇した。
As a result, the mixture (M execution composition) immediately gave off its latent heat and rose to 55°C.

プロピレングリコールを約7.4重量%添加した上記混
合物は、移動する際力゛ラス壁から落ちた結iでは誘発
されなかったが、先のとがった金属棒        
    ゝ1で強く押すと誘発された。
The above mixture containing approximately 7.4% by weight of propylene glycol was not induced by the force of falling from the glass wall while moving, but was
ゝIt was triggered when I pressed hard in 1.

この混合物について、実施例1と同様に60回溶解、固
化及び誘発を繰り返したが、全て実施例1と同様の結果
が得られ、また、この混合物は、80℃の粘稠溶液とし
た場合にヒドロキシプロピル化グアーガムの凝集、分離
もなく、良好な粘稠度を保持していた。
This mixture was repeatedly dissolved, solidified, and induced 60 times in the same manner as in Example 1, and the same results as in Example 1 were obtained. There was no aggregation or separation of the hydroxypropylated guar gum, and good consistency was maintained.

更に、混合物を実施例1と同様室温で100日間保持後
、誘発を行ったが、混合物は誘発後直ちに55℃に上昇
した。その後、この混合物について溶解、固化及び誘発
を繰り返し10回行ったが、すべて55℃に上昇した。
Furthermore, induction was performed after the mixture was kept at room temperature for 100 days as in Example 1, but the temperature of the mixture rose to 55° C. immediately after induction. Thereafter, this mixture was repeatedly melted, solidified, and induced 10 times, all raising the temperature to 55°C.

〔発明の効果〕〔Effect of the invention〕

本発明の蓄熱剤組成物は、室温では、加熱により蓄熱し
た潜熱を安定な過冷却状態で保持しており、過冷却状態
を破壊すれば潜熱を放出するもので、上記の加熱・過冷
却破壊(混合物の熔解、固化及び誘発)を繰り返し行う
ことにより1.上記の蓄熱・放熱作用が繰り返して行わ
れるから、本発明の蓄熱剤組成物によれば、必要な時に
潜熱を取り出すことができ、不必要時に放熱する惧れが
なく、且つ繰り返し使用が可能である。
At room temperature, the heat storage agent composition of the present invention retains the latent heat accumulated through heating in a stable supercooled state, and when the supercooled state is broken, the latent heat is released. By repeating (melting, solidifying and inducing the mixture) 1. Since the above-mentioned heat storage and heat dissipation actions are performed repeatedly, the heat storage agent composition of the present invention can extract latent heat when necessary, there is no risk of heat dissipation when unnecessary, and it can be used repeatedly. be.

Claims (1)

【特許請求の範囲】[Claims] 過冷却可能で、高温相から低温相に移転する際に潜熱を
放出する塩水和物と、ヒドロキシプロピル化グアーガム
とを必須の構成成分として含有する過冷却可能な蓄熱剤
組成物。
A supercoolable heat storage agent composition containing as essential constituents a salt hydrate that is supercoolable and releases latent heat when transferring from a high temperature phase to a low temperature phase, and hydroxypropylated guar gum.
JP59135879A 1984-06-30 1984-06-30 Thermal energy storage material composition Pending JPS6114283A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59135879A JPS6114283A (en) 1984-06-30 1984-06-30 Thermal energy storage material composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59135879A JPS6114283A (en) 1984-06-30 1984-06-30 Thermal energy storage material composition

Publications (1)

Publication Number Publication Date
JPS6114283A true JPS6114283A (en) 1986-01-22

Family

ID=15161905

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59135879A Pending JPS6114283A (en) 1984-06-30 1984-06-30 Thermal energy storage material composition

Country Status (1)

Country Link
JP (1) JPS6114283A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62205184A (en) * 1986-03-05 1987-09-09 Mitsui Petrochem Ind Ltd Heat energy storing material
JPS63101473A (en) * 1986-10-06 1988-05-06 アメリカ合衆国 Heat energy storage composition
JPS63137628U (en) * 1987-03-04 1988-09-09
JPH01164365A (en) * 1987-12-22 1989-06-28 Yamato Seisakusho:Kk Portable heat insulating device
WO2014024883A1 (en) * 2012-08-08 2014-02-13 古河電気工業株式会社 Heat storage material composition, auxiliary heat source using same, and heat supply method
WO2014050158A1 (en) * 2012-09-28 2014-04-03 トッパン・フォームズ株式会社 Cooling tool
JP2015183973A (en) * 2014-03-26 2015-10-22 古河電気工業株式会社 Supercooling-type latent heat storage material composition and heat storage system
JP2016020470A (en) * 2013-09-30 2016-02-04 パナソニック株式会社 Thermal storage material composition and method for using thermal storage material composition
JP2017052953A (en) * 2016-09-21 2017-03-16 トッパン・フォームズ株式会社 Cold insulation tool
TWI632335B (en) * 2012-09-28 2018-08-11 凸版福姆斯股份有限公司 Cooling pack

Cited By (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62205184A (en) * 1986-03-05 1987-09-09 Mitsui Petrochem Ind Ltd Heat energy storing material
JPS63101473A (en) * 1986-10-06 1988-05-06 アメリカ合衆国 Heat energy storage composition
JPS63137628U (en) * 1987-03-04 1988-09-09
JPH0416661Y2 (en) * 1987-03-04 1992-04-14
JPH01164365A (en) * 1987-12-22 1989-06-28 Yamato Seisakusho:Kk Portable heat insulating device
JPWO2014024883A1 (en) * 2012-08-08 2016-07-25 古河電気工業株式会社 Heat storage material composition, auxiliary heat source and heat supply method using the same
WO2014024883A1 (en) * 2012-08-08 2014-02-13 古河電気工業株式会社 Heat storage material composition, auxiliary heat source using same, and heat supply method
US10359237B2 (en) 2012-08-08 2019-07-23 Furukawa Electric Co., Ltd. Heat source material composition, and auxiliary heat source and heat supply method using the same
WO2014050158A1 (en) * 2012-09-28 2014-04-03 トッパン・フォームズ株式会社 Cooling tool
CN104662119A (en) * 2012-09-28 2015-05-27 凸版资讯股份有限公司 Cooling tool
TWI632335B (en) * 2012-09-28 2018-08-11 凸版福姆斯股份有限公司 Cooling pack
JP2014070141A (en) * 2012-09-28 2014-04-21 Toppan Forms Co Ltd Cooling tool
JP2016020470A (en) * 2013-09-30 2016-02-04 パナソニック株式会社 Thermal storage material composition and method for using thermal storage material composition
JP2015183973A (en) * 2014-03-26 2015-10-22 古河電気工業株式会社 Supercooling-type latent heat storage material composition and heat storage system
JP2017052953A (en) * 2016-09-21 2017-03-16 トッパン・フォームズ株式会社 Cold insulation tool

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