JPS58176291A - Thermal energy storage material composition - Google Patents
Thermal energy storage material compositionInfo
- Publication number
- JPS58176291A JPS58176291A JP5945182A JP5945182A JPS58176291A JP S58176291 A JPS58176291 A JP S58176291A JP 5945182 A JP5945182 A JP 5945182A JP 5945182 A JP5945182 A JP 5945182A JP S58176291 A JPS58176291 A JP S58176291A
- Authority
- JP
- Japan
- Prior art keywords
- formate
- calcium
- energy storage
- storage material
- thermal energy
- 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
Links
Abstract
Description
【発明の詳細な説明】
して使用される酢酸ナトリウム3水塩の性能改善に関す
る。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to improving the performance of sodium acetate trihydrate used as a compound.
酢酸ナトリウム3水塩は融点が58℃、融解熱が単位重
量当り6 0 cal/P s単位体積当り87c峰仕
という特性をもち、太陽熱を利用する蓄熱材としてその
実用化が期待される化合物である。Sodium acetate trihydrate has a melting point of 58°C and a heat of fusion of 60 cal/Ps per unit weight and 87c per unit volume, and is a compound that is expected to be put to practical use as a heat storage material that utilizes solar heat. be.
しかし、融解蓄熱−凝固放熱のヒートサイクルを長期に
わたってくり返すと、系に酢酸ナトリウム無水塩の結晶
が徐々に析出してくる。該無水塩の生成自体はヒートサ
イクルの支障にはならないが、これが次第に大量となり
系の底部に沈澱堆積し初めると、いわゆる相分離現象が
おこり効率的な熱の取り出しが不可能となるのでその解
決が必要である。However, when the heat cycle of melting heat storage and solidification heat release is repeated over a long period of time, crystals of sodium acetate anhydride gradually precipitate in the system. The production of anhydrous salt itself does not interfere with the heat cycle, but when it gradually increases in large quantities and begins to precipitate and accumulate at the bottom of the system, a so-called phase separation phenomenon occurs, making efficient heat extraction impossible. is necessary.
かかる対策として酢酸ナトリウム5水塩にゲル化剤を配
合したり、あるいは酢酸ナトリウム6水塩をカプセル化
する等の方法が提案されている力ζその効果は必ずしも
充分ではない。As a countermeasure against this problem, methods such as adding a gelling agent to sodium acetate pentahydrate or encapsulating sodium acetate hexahydrate have been proposed, but their effects are not necessarily sufficient.
しかるに本発明者等はかかる問題を解決すべく鋭意研究
を重ねた結果、酢酸ナトリウムろ水塩にギ酸アンモニウ
ム、ギ酸カリウム、ギ酸銅、ギ酸マンガン、ギ酸カルシ
ウム、硝酸カルシウム、酢酸カルシウム、ハロゲン化カ
ルシウムの群から選ばれる少くとも一種の化合物を配合
した蓄熱材組成物は、長期にわたって蓄熱−放熱のヒー
トサイクルをくり返しても酢酸ナトリウム無水塩の析出
、沈澱による相分離が全くおこらず効率的な熱交換が実
施出来ると共に、上記化合物の添加によって酢酸ナトリ
ウム6水塩の凝固点が若干低下するので、比較的安価な
集熱器を使用しても効率良く、所定量の熱量を取得する
ことが出来る等の顕著な効果を奏し得ることを見出し本
発明を完成する番こ到った。However, as a result of extensive research in order to solve this problem, the present inventors found that ammonium formate, potassium formate, copper formate, manganese formate, calcium formate, calcium nitrate, calcium acetate, and calcium halides were added to sodium acetate filtrate. A heat storage material composition containing at least one compound selected from the group allows efficient heat exchange without precipitation of sodium acetate anhydride or phase separation due to precipitation even after repeated heat storage-radiation heat cycles over a long period of time. In addition, the addition of the above compound slightly lowers the freezing point of sodium acetate hexahydrate, so even if a relatively inexpensive heat collector is used, it is possible to efficiently obtain a predetermined amount of heat. Having discovered that it can produce remarkable effects, the time has come to complete the present invention.
本発明で使用する化合物は無水物あるLlま水和塩のい
ずれも使用可能である。又その中でノ10ゲン化カルシ
ウムとは塩化カルシウムや臭化カルシウム、ヨウ化カル
シウム等である。塩化カルシウムとしては無水塩、1水
塩、2水塩、4水塩、6水塩等いずれも使用可能である
。本発明の化合物は単独でも又、21[以上を併用して
も差支えな(Ao特に好適な化合物としてはギ酸カルシ
ウム、硝酸カルシウム4水塩が挙げられる。The compounds used in the present invention can be either anhydrous, hydrated, or anhydrous. Among these, calcium 10genide includes calcium chloride, calcium bromide, calcium iodide, and the like. As calcium chloride, any anhydrous salt, monohydrate salt, dihydrate salt, tetrahydrate salt, hexahydrate salt, etc. can be used. The compounds of the present invention may be used alone or in combination with 21 or more (Ao) Particularly preferred compounds include calcium formate and calcium nitrate tetrahydrate.
かかる化合物以外にも、例えばギ酸タリウム、ギ酸クロ
ム、ギ酸タリウム、ギ酸ゲラニル、ギ酸セシウム、ギ酸
タリウム、ギ酸ニッケル等も相分離防止効果はかなりあ
るが毒性の点で実用性番こ乏しい。In addition to such compounds, for example, thallium formate, chromium formate, thallium formate, geranyl formate, cesium formate, thallium formate, nickel formate, etc. have a considerable effect on preventing phase separation, but are of little practical use in terms of toxicity.
該化合物の配合量は組成物全体に対して0.1〜10重
量憾好ましくは0.5〜2.0重量幅の範囲から選ばれ
る。0.1重量幅以下では効果に乏しく、一方10重量
参以上では蓄熱量の低下が右こる。The compounding amount of the compound is selected from the range of 0.1 to 10% by weight, preferably 0.5 to 2.0% by weight based on the entire composition. If the width is less than 0.1 weight, the effect will be poor, while if it is more than 10 weight, the amount of heat storage will decrease.
蓄熱材組成物の調製に際しては少量の他の蓄熱材、蓄熱
助剤等の任意の成分の併用も可能である。When preparing the heat storage material composition, it is also possible to use small amounts of other arbitrary components such as other heat storage materials and heat storage aids.
かくして得られる蓄熱材組成物は太陽熱を利用するソー
ラーシステムの暖房用に好適に用いられ、長期にわたっ
て安定なヒートサイクルを実施することが可能である。The heat storage material composition obtained in this way is suitably used for heating in a solar system that utilizes solar heat, and can perform a stable heat cycle over a long period of time.
次に実例を挙げて本発明の蓄熱材を更に具体的に説明す
る。Next, the heat storage material of the present invention will be explained in more detail by giving examples.
実例1
酢酸ナトリウム6水塩49.S Pとギ酸カルシウム0
.5 Fの混合物(凝固点56℃)を大型試験官に入れ
80℃に加熱して均一溶液とした。更に水分蒸発防止の
ため流動パラフィン5−を加えた。Example 1 Sodium acetate hexahydrate 49. SP and calcium formate 0
.. A mixture of 5 F (freezing point: 56°C) was placed in a large test tube and heated to 80°C to form a homogeneous solution. Furthermore, liquid paraffin 5- was added to prevent moisture evaporation.
2時間後この組成□物を0.25 T/*の速度で冷却
し50℃番こなった時点で微量の核結晶を加えて固化さ
せる。その後再び80℃に昇温し2時間この温度に保持
したのち、冷却を開始し同様の操作を行った。このヒー
トサイクルを500回くり返したが相分離は全く認めら
れなかった。対照例としてギ酸カルシウムの使用を省略
したところ、20回のヒートサイクルで相分離が認めら
れ組成物の騒を無水酢酸ナトリウム結晶が占めた。After 2 hours, this composition □ was cooled at a rate of 0.25 T/*, and when it reached 50°C, a small amount of core crystals were added to solidify it. Thereafter, the temperature was raised to 80° C. again and maintained at this temperature for 2 hours, then cooling was started and the same operation was performed. This heat cycle was repeated 500 times, but no phase separation was observed. As a control example, when the use of calcium formate was omitted, phase separation was observed after 20 heat cycles, and anhydrous sodium acetate crystals accounted for the noise in the composition.
実例2〜9
表に示す如き化合物を用いて実例1と同一の実験を行っ
た。その結果を表に示す。Examples 2 to 9 The same experiments as in Example 1 were conducted using the compounds shown in the table. The results are shown in the table.
Claims (1)
ウム、ギ酸銅、ギ酸マンガン、ギ酸カルシウム、硝酸カ
ルシウム、酢酸カルシウム、ノ10ゲン化カルシウムの
群から選ばれる少くとも一種の化合物を配合してなる蓄
熱材組成物。A heat storage material made by blending sodium acetate trihydrate with at least one compound selected from the group of ammonium formate, potassium formate, copper formate, manganese formate, calcium formate, calcium nitrate, calcium acetate, and calcium chloride. Composition.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5945182A JPS58176291A (en) | 1982-04-08 | 1982-04-08 | Thermal energy storage material composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5945182A JPS58176291A (en) | 1982-04-08 | 1982-04-08 | Thermal energy storage material composition |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS58176291A true JPS58176291A (en) | 1983-10-15 |
Family
ID=13113668
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5945182A Pending JPS58176291A (en) | 1982-04-08 | 1982-04-08 | Thermal energy storage material composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS58176291A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004061044A1 (en) * | 2003-01-02 | 2004-07-22 | Rubitherm Gmbh | Phase change temperature controlling material and method for the production thereof |
DE102013224448A1 (en) * | 2013-11-28 | 2015-05-28 | Siemens Aktiengesellschaft | Phase change material and use thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5314173A (en) * | 1976-07-26 | 1978-02-08 | Mitsubishi Electric Corp | Heat regenerating material |
JPS55142078A (en) * | 1979-04-23 | 1980-11-06 | Sekisui Chem Co Ltd | Heat-storing composition |
JPS5893779A (en) * | 1981-11-30 | 1983-06-03 | Nippon Synthetic Chem Ind Co Ltd:The | Thermal energy storing composition |
-
1982
- 1982-04-08 JP JP5945182A patent/JPS58176291A/en active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5314173A (en) * | 1976-07-26 | 1978-02-08 | Mitsubishi Electric Corp | Heat regenerating material |
JPS55142078A (en) * | 1979-04-23 | 1980-11-06 | Sekisui Chem Co Ltd | Heat-storing composition |
JPS5893779A (en) * | 1981-11-30 | 1983-06-03 | Nippon Synthetic Chem Ind Co Ltd:The | Thermal energy storing composition |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2004061044A1 (en) * | 2003-01-02 | 2004-07-22 | Rubitherm Gmbh | Phase change temperature controlling material and method for the production thereof |
DE102013224448A1 (en) * | 2013-11-28 | 2015-05-28 | Siemens Aktiengesellschaft | Phase change material and use thereof |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS6324555B2 (en) | ||
JPS58176291A (en) | Thermal energy storage material composition | |
JP3442155B2 (en) | Heat storage material composition | |
KR20050005467A (en) | Heat-storage medium ii | |
JP2001031956A (en) | Latent heat storage material composition | |
JP4309991B2 (en) | Thermal storage material composition and heating device using the same | |
JPH0352511B2 (en) | ||
JP4252118B2 (en) | Method for producing supercooling inhibitor of salt hydrate | |
JPS59543B2 (en) | heat storage material | |
EP0092199B1 (en) | Heat storage material | |
JP3880677B2 (en) | Latent heat storage material composition | |
JPH0157157B2 (en) | ||
JPS5952920B2 (en) | Latent heat storage material | |
JPS61197668A (en) | Thermal energy storage material | |
JPS6151079A (en) | Thermal energy storage material | |
JPS6251311B2 (en) | ||
JPH0134475B2 (en) | ||
JPS6044578A (en) | Thermal energy storage material | |
JPS5938276A (en) | Heat storage material | |
JPS6111986B2 (en) | ||
JPS6058480A (en) | Heat storage material | |
JPS63137982A (en) | Heat storage material composition | |
JPH0562158B2 (en) | ||
JPS58195796A (en) | Heat accumulating material for use in space heating | |
JPS6111275B2 (en) |