JPS5941382A - Heat storage material - Google Patents
Heat storage materialInfo
- Publication number
- JPS5941382A JPS5941382A JP15224982A JP15224982A JPS5941382A JP S5941382 A JPS5941382 A JP S5941382A JP 15224982 A JP15224982 A JP 15224982A JP 15224982 A JP15224982 A JP 15224982A JP S5941382 A JPS5941382 A JP S5941382A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- dihydrate
- calcium chloride
- storage material
- heat storage
- 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,更に詳細には放熱速度の速い塩化カルシウムー水系
蓄熱材に関するものである。DETAILED DESCRIPTION OF THE INVENTION More specifically, the present invention relates to a calcium chloride water-based heat storage material that has a high heat dissipation rate.
従来より塩化カルンウムー水系蓄熱材とじては,塩化カ
ルンウム6水塩( OaOj!!2− 61120)が
注目されてきたが,塩化カルシウム6水塩は過冷却が太
きいといった蓄熱材としての大きな欠点を有していた。Carunium chloride hexahydrate (OaOj!!2-61120) has traditionally attracted attention as a water-based heat storage material based on calcium chloride, but calcium chloride hexahydrate has major drawbacks as a heat storage material such as excessive supercooling. had.
そこで過冷却防止対策として各種添加物が提案され,過
冷却は軽減されて・さている。しかし乍ら,塩化カルシ
ウムろ水塩は結晶化速度が遅いため,長周期(週〜季節
)の蓄放熱には適しているが,短周期(時間〜日)の蓄
放熱には適さ彦いといった問題があった。Therefore, various additives have been proposed as measures to prevent supercooling, and supercooling has been reduced. However, because calcium chloride filtrate has a slow crystallization rate, it is suitable for heat storage and release over long periods (weeks to seasons), but not suitable for short periods (hours to days). There was a problem.
本発明者キは上述した短周期(時間〜日)に適した結晶
化速度の速い蓄熱材を得るべく鋭意研究を重ねた結果,
一定の濃度範囲の塩化カルシウム溶液に沈降防止剤を添
加することにより。As a result of intensive research to obtain a heat storage material with a fast crystallization rate suitable for the above-mentioned short period (hours to days), the inventor Ki has found that
By adding an anti-settling agent to a calcium chloride solution in a certain concentration range.
優れた特性を有する蓄熱材が得られることを見い出し.
本発明を完成したものである。即ち。It was discovered that a heat storage material with excellent properties can be obtained.
This completes the present invention. That is.
本発明は塩化カルシウムの量が水溶液中558〜75.
2重量係である塩化カルシウム水溶液と沈降防止剤とか
ら少なくともなることを特徴とする蓄熱材を要旨とする
ものである。In the present invention, the amount of calcium chloride in the aqueous solution is 558 to 75.
The gist of the present invention is a heat storage material comprising at least a calcium chloride aqueous solution having a weight ratio of 2 and an anti-settling agent.
本発明の蓄熱材が何故、結晶化速度が速く。The reason why the heat storage material of the present invention has a fast crystallization speed.
短周期(時間〜日)使用に適しているのかは定かではな
いが以下の様に推察される。It is not certain whether it is suitable for short-term use (hours to days), but it is inferred as follows.
本発明の蓄熱材は塩化カル7ウムの量が水溶液中55.
8〜752重量係で重量塩化カルシウム水溶液を基材と
しているため、塩化カルシウム−水系平衡状態図(第1
図参照)における塩化カルシウム4水塩の固相線1以上
、液相線2以下の温度範囲においては塩化カルンウム2
水塩結晶と、塩化カルシウム溶液の2相が共存し。In the heat storage material of the present invention, the amount of calcium chloride in the aqueous solution is 55.
Since the base material is a calcium chloride aqueous solution, the calcium chloride-water system equilibrium state diagram (first
Calunium chloride 2
Two phases coexist: hydrate crystals and calcium chloride solution.
沈降防止剤の増粘もしくは結晶とのからみ合い効果によ
り、塩化カル/ラム2水塩の沈降を防止するため、塩化
カルシウム水溶液相に塩化カルシウム2水塩結晶が均一
に分散されており。Calcium chloride dihydrate crystals are uniformly dispersed in the calcium chloride aqueous solution phase in order to prevent calcium chloride/rum dihydrate from settling due to the thickening effect of the antisettling agent or the entanglement effect with the crystals.
その結果冷却時塩化カル/ウム2水塩を核として塩化カ
ルシウム4水塩の結晶成長が速やかに行なわれるものと
思われる。As a result, it is thought that upon cooling, crystal growth of calcium chloride tetrahydrate occurs rapidly using calcium chloride dihydrate as the nucleus.
以下に本発明に使用する各成分について説明する。Each component used in the present invention will be explained below.
塩化カルシウムは水と混合して、塩化カルシウム水溶液
を得るためのものであり、無水塩。Calcium chloride is an anhydrous salt that can be mixed with water to obtain a calcium chloride aqueous solution.
2水塩、4水塩が使用でき、その使用量は塩化カルシウ
ム水溶液中、無水塩換算で558〜75258〜752
重量部88重量φより少ないと過冷却が大きくなるとい
った問題があり。Dihydrate salt and tetrahydrate salt can be used, and the amount used is 558 to 75258 to 752 in terms of anhydrous salt in calcium chloride aqueous solution.
If the weight part is less than 88 weight φ, there is a problem that supercooling becomes large.
75252重量部多いと融点が高くなり蓄熱材として使
用できなくなる。If the amount exceeds 75252 parts by weight, the melting point will become too high to be used as a heat storage material.
次に沈降防止剤としてはアスベスト粉、カオリン土、微
粉末シリカ、微粉末アルミナ、ノリ力ゲル、ケイソウ土
、ガラス粉、雲母粉の中の1種もしくは2種以上が使用
でき、その使用量は蓄熱材全量に対して1〜30重量係
重量ましい。1重量部より少ないと効果がなく、塩化カ
ルシウム2水塩結晶が沈降してしまうといった問題が生
じ、300重量部り多いと蓄熱量が低下するといった問
題が生じる。Next, as an anti-settling agent, one or more of asbestos powder, kaolin earth, finely powdered silica, finely powdered alumina, Noriyoku gel, diatomaceous earth, glass powder, and mica powder can be used, and the amount used is It is preferably 1 to 30% by weight based on the total amount of the heat storage material. If it is less than 1 part by weight, there will be no effect, causing a problem that calcium chloride dihydrate crystals will settle, and if it is more than 300 parts by weight, a problem will occur such that the amount of heat storage decreases.
尚、上記成分以外に一般に使用されている結晶核^や、
熱良導体などの添加物を適宜添加することもできる。In addition to the above ingredients, commonly used crystal nuclei^,
Additives such as good thermal conductors can also be added as appropriate.
次に本発明の蓄熱材の製造方法を簡単に述べる。Next, the method for manufacturing the heat storage material of the present invention will be briefly described.
先ず、塩化カル/ラム(2水塩、4水塩を含む)と水と
沈降防止剤を必要量混合し、加熱攪拌し、均一な液体と
すればよく、必要に応じて。First, the necessary amounts of Cal/Rum chloride (including dihydrate and tetrahydrate salts), water, and anti-settling agent are mixed, and the mixture is heated and stirred to form a homogeneous liquid, if necessary.
結晶核形成剤や熱良導体などの添加物を適宜添加しても
よいものである。Additives such as a crystal nucleating agent and a good thermal conductor may be added as appropriate.
次に本発明の蓄放熱状態を第1図を用いて説明する。Next, the heat storage/dissipation state of the present invention will be explained using FIG. 1.
本発明の蓄熱材を加熱して行くと、塩化カルシウム4水
塩及び2水塩の各々の比熱に応じた顕熱を蓄熱し、温度
が第1図における塩化カルシウム4水塩の固相線1に達
すると、4水塩が融解潜熱を蓄熱しつつ融解し液相とな
り、2水塩と液相が共存状態となり、2水塩粒子が沈降
防止剤の作用で沈降せずに液中に均一に分散している。When the heat storage material of the present invention is heated, it stores sensible heat corresponding to the specific heat of each of calcium chloride tetrahydrate and dihydrate, and the temperature rises to the solidus line 1 of calcium chloride tetrahydrate in FIG. When this temperature is reached, the tetrahydrate accumulates the latent heat of fusion and melts into a liquid phase, and the dihydrate and liquid phase coexist, and the dihydrate particles do not settle due to the action of the anti-settling agent and are uniformly distributed in the liquid. are distributed in
更に加熱を続けると第1図における液相線2まで2水塩
と液相の各々の比熱に応じた顕熱を蓄熱していく5次に
冷却していくと、固相線1までは顕熱を放熱し、固相線
1に達すると、わずかに過冷却を示した後に2水塩粒子
を核として4水塩が融解潜熱を放熱しつつ析出し。If heating is continued further, sensible heat corresponding to the specific heat of the dihydrate and liquid phase will be accumulated up to liquidus line 2 in Figure 1.5 When cooling is continued, sensible heat will be accumulated up to solidus line 1. When the heat is radiated and the solidus line 1 is reached, there is a slight supercooling, and then tetrahydrate is precipitated with the dihydrate particles as the nucleus while radiating the latent heat of fusion.
同相となり、それ以後は同相の顕熱を放熱して行く。They become the same phase, and from then on, the sensible heat of the same phase is dissipated.
次に本発明を実施例により詳細に説明する。Next, the present invention will be explained in detail with reference to examples.
実施例中「部」とあるのは「重量部」を示す。In the examples, "parts" indicate "parts by weight."
実施例 1
塩化カルシウム 72部、k
′°部カオリン土
Z2部上記各成分を混合し、加
熱(70℃)攪拌して蓄熱材を得た。Example 1 Calcium chloride 72 parts, k
'° part kaolin soil
Part Z2 The above components were mixed and heated (70° C.) and stirred to obtain a heat storage material.
実施例 2
塩化力ルンウム 72部水
28部蝋旬末シυ力 6・
6部上記各成分を実施例1と同様にして蓄熱材を得た。Example 2 Chloride 72 parts water
Part 28 Wax Season End Shiυ Power 6.
6 parts A heat storage material was obtained using the same ingredients as in Example 1.
実施例 6
塩化カル/ラム 72部水
28部ケインウ土 1
2部上記各成分を実施例1と同様にして蓄熱材を得た。Example 6 Cal chloride/rum 72 parts water
28th division Keinwu soil 1
2 parts A heat storage material was obtained using the above components in the same manner as in Example 1.
実施例 4
塩化カルシウム 72部水
28部アスベスト粉
12部」二記各成分を実施例1と同様にして蓄熱材を得
た。Example 4 Calcium chloride 72 parts water
28 parts asbestos powder
A heat storage material was obtained in the same manner as in Example 1 using the same ingredients as in Example 1.
比較例 1
塩化カルシウム 72部水
28部上記各成分を実施例1と同様にして蓄熱
材を得た。Comparative example 1 Calcium chloride 72 parts water
28 parts A heat storage material was obtained using the same ingredients as in Example 1.
比較例 2
塩化カルシウム6水塩 ioo部塩化スト
ロンチウム6水塩 5部カオリン土
10部上記上記発成実施例
1と同様にして蓄熱刊を得た。Comparative Example 2 Calcium chloride hexahydrate IOO parts Strontium chloride hexahydrate 5 parts Kaolin earth
10 copies of heat storage paper were obtained in the same manner as in Example 1 above.
実施例1〜4.比較例1.2で得られた蓄熱材の試験結
果を表−1に示す。Examples 1-4. Table 1 shows the test results of the heat storage material obtained in Comparative Example 1.2.
表 −1
(注1)・・10分以上で放熱がなく、相分離をおこし
た。Table 1 (Note 1): There was no heat release for more than 10 minutes, and phase separation occurred.
(注2)・・・10分以上で放熱がなかった。(Note 2)...There was no heat radiation for 10 minutes or more.
※1・・・実施例1〜4.比較例1.2で得られた蓄熱
材5f/を内径10Mの試験管に充填し。*1...Examples 1 to 4. A test tube with an inner diameter of 10 M was filled with 5 f/ of the heat storage material obtained in Comparative Example 1.2.
中央に熱電対を付けたゴム栓で密封し、70℃と25°
Cに保ったウォーターバス間で加熱冷却ザイクルを10
0回繰り返し、1回目、10回目、100回目における
凝固点と冷却開始から凝固が完了する1での時間を測定
した。Seal with a rubber stopper with a thermocouple attached to the center, 70°C and 25°
10 heating and cooling cycles between water baths maintained at C.
It was repeated 0 times, and the freezing point at the 1st, 10th, and 100th times and the time from the start of cooling to 1 when solidification was completed were measured.
以上に示すよう本発明の蓄熱材は放熱速度が速く、短周
期(時間〜日)の使用に適し、経時的な繰り返し使用に
耐えうる。優れたものであり、ソーラーコレクターや暖
房用等の迅速な放熱を必要とする蓄熱材として好適なも
のである。As shown above, the heat storage material of the present invention has a high heat dissipation rate, is suitable for short-term use (hours to days), and can withstand repeated use over time. It is an excellent material and is suitable as a heat storage material for solar collectors, heating, etc. that requires rapid heat dissipation.
第1図は塩化カルシウム−水系の平衡状態図である。
1・・・・・塩化カルシウム4水塩の固相線2・・・・
・・液 相 線
特許出願人 べんてる株式会社FIG. 1 is an equilibrium diagram of the calcium chloride-water system. 1... Solidus line of calcium chloride tetrahydrate 2...
...Liquid phase line patent applicant Bentel Co., Ltd.
Claims (1)
重量係である塩化カル/ラム水溶液と沈降防止剤とから
少々くともなることを特徴とする蓄熱材。 +21前記沈降防止剤がアスベスト粉、カオリン土。 微粉末/リカ、微粉末アルミナ、シリカゲル。 ケイソウ土、ガラス粉、雲母粉の中の1種もしくは2種
以上である特許請求の範囲第(1)項記載の蓄熱材。(1) The amount of calcium chloride in the aqueous solution is 558 to 75.2
A heat storage material characterized by being slightly cloudy due to the weight factor Cal chloride/rum aqueous solution and anti-settling agent. +21 The anti-settling agent is asbestos powder or kaolin soil. Fine powder/Rica, fine powder alumina, silica gel. The heat storage material according to claim 1, which is one or more of diatomaceous earth, glass powder, and mica powder.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15224982A JPS5941382A (en) | 1982-08-31 | 1982-08-31 | Heat storage material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15224982A JPS5941382A (en) | 1982-08-31 | 1982-08-31 | Heat storage material |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5941382A true JPS5941382A (en) | 1984-03-07 |
Family
ID=15536351
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15224982A Pending JPS5941382A (en) | 1982-08-31 | 1982-08-31 | Heat storage material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5941382A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3003867A1 (en) * | 2013-03-29 | 2014-10-03 | Hevatech | COMPOSITION FOR THE STORAGE AND PRODUCTION OF THERMO-CHEMICAL ENERGY, METHOD FOR STORING AND PRODUCING THERMO-CHEMICAL ENERGY, AND DEVICE FOR PRODUCING THERMO-CHEMICAL ENERGY |
-
1982
- 1982-08-31 JP JP15224982A patent/JPS5941382A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR3003867A1 (en) * | 2013-03-29 | 2014-10-03 | Hevatech | COMPOSITION FOR THE STORAGE AND PRODUCTION OF THERMO-CHEMICAL ENERGY, METHOD FOR STORING AND PRODUCING THERMO-CHEMICAL ENERGY, AND DEVICE FOR PRODUCING THERMO-CHEMICAL ENERGY |
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