JPS6281481A - Latent heat storing material - Google Patents

Latent heat storing material

Info

Publication number
JPS6281481A
JPS6281481A JP60220681A JP22068185A JPS6281481A JP S6281481 A JPS6281481 A JP S6281481A JP 60220681 A JP60220681 A JP 60220681A JP 22068185 A JP22068185 A JP 22068185A JP S6281481 A JPS6281481 A JP S6281481A
Authority
JP
Japan
Prior art keywords
latent heat
melting
storing material
heat storing
temp
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.)
Granted
Application number
JP60220681A
Other languages
Japanese (ja)
Other versions
JPH0641587B2 (en
Inventor
Takeshi Takeda
竹田 武司
Ikuhiko Machida
町田 育彦
Yasuo Kudo
康夫 工藤
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 JP60220681A priority Critical patent/JPH0641587B2/en
Publication of JPS6281481A publication Critical patent/JPS6281481A/en
Publication of JPH0641587B2 publication Critical patent/JPH0641587B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Abstract

PURPOSE:To provide a latent heat storing material which is free from toxicity and corrosive properties and is incombustible and melts at about 25 deg.C and which comprises Na2SO4.10H2O and MgSO4.7H2O. CONSTITUTION:1mol of Na2SO4.10H2O is blended with 0.7-1.5mol of MgSO4.7 H2O and, if necessary, a phase separation inhibitor (e.g., crosslinked acrylic acid polymer) and an undercooling inhibitor (e.g., borax), thereby adjusting the melting initiation temp. to 22.0 deg.C or above and the melting completion temp. to 28 deg.C or below and obtaining a latent heat storing material useful for temp. adjustment of hermetically sealed space in which electronic equipment is installed.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、電子機器などを設置した密閉空間の温度調節
に用いられる潜熱蓄熱材に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a latent heat storage material used for temperature control in a closed space in which electronic equipment and the like are installed.

従来の技術 動作中に発熱をするたとえば交換器の様な電子機器を設
置した密閉空間の温度は、夏期の日中には30℃を越え
る外気温と機器からの放熱によっ2 ページ で50℃程度にまで達する事があり、電子部品の安定動
作のため空調機器を使用し30℃程度を越えない様に調
節されている。省エネルギーを達成しつ\斯かる空調を
行なうには潜熱蓄熱材の適用が有効であり、その検討が
行なわれつ\ある。
Conventional technologyThe temperature in a closed space where electronic equipment such as an exchanger that generates heat during operation can reach 50°C during the day due to the outside temperature exceeding 30°C and the heat radiated from the equipment. In order to ensure stable operation of electronic components, air conditioners are used to keep temperatures below 30°C. In order to achieve such air conditioning while achieving energy savings, it is effective to apply latent heat storage materials, and studies are currently underway.

発明が解決しようとする問題点 被空調空間の温度を30℃程度に調節するには、潜熱蓄
熱材の融点は25℃程度以下にある事が必要である。当
然の本年ら融点の低い潜熱蓄熱材を用いる程被空調空間
の温度を低く設定する事が可能となり上記目的の達成が
容易となるが、夜間外気と熱交換し外気に放熱して凝固
し翌日の吸熱・融解にそなえる事が困難となる。夜間の
外気温度を20℃程度と想定した場合、結局25℃程度
の融点が最適となる。
Problems to be Solved by the Invention In order to adjust the temperature of the air-conditioned space to approximately 30°C, the melting point of the latent heat storage material must be approximately 25°C or lower. Naturally, the more latent heat storage materials with lower melting points are used, the lower the temperature of the air-conditioned space can be set, making it easier to achieve the above objective. It becomes difficult to prepare for heat absorption and melting the next day. If the outside temperature at night is assumed to be about 20°C, the optimal melting point will be about 25°C.

数多くの潜熱蓄熱材のうちで、価格、不燃性、毒性、腐
蝕性などの面から最も実用的と考えられているものの1
つに硫酸ナトリウム10水塩(Na2804・]0H2
0)がある。この材料の融点は32℃にあるため、上記
目的に対しては適当でなく融点を3 ペー、・ 25℃程度に低下せしy)る必要がある。
Among the many latent heat storage materials, this is one of the most practical in terms of price, nonflammability, toxicity, and corrosivity.
Sodium sulfate decahydrate (Na2804・]0H2
0). Since the melting point of this material is 32°C, it is not suitable for the above purpose and it is necessary to lower the melting point to about 25°C.

本発明は、上記問題点を解決しNa 2804・I 0
T(20を主材とした融点25℃程度の潜熱蓄熱材を提
供する目的でなされたものである。
The present invention solves the above problems and solves the problems described above.
It was made for the purpose of providing a latent heat storage material with a melting point of about 25°C, which is based on T(20).

問題点を解決するための手段 本発明による潜熱蓄熱拐は、Na2SO4−10I−(
20と硫酸マグネシウム7水塩(M9804・7 ’F
I20 )とを少なくとも含む構成により上記目的を達
成することができる。
Means for Solving the Problems The latent heat storage according to the present invention can be applied to Na2SO4-10I-
20 and magnesium sulfate heptahydrate (M9804.7'F
The above object can be achieved by a configuration including at least I20).

作    用 本発明におイT Mg804−7 HzOはNa2SO
4・10I■20の融点を低下せしめる作用をし、Na
 2 SO4・1011201モルに対しMqSO4・
71120を07モル乃至15モル混合した場合には融
点は約25℃となった。
Effects of the present invention Mg804-7 HzO is Na2SO
4.10I■20 has the effect of lowering the melting point, and Na
2 MqSO4・for SO4・1011201 mol
When 07 to 15 moles of 71120 were mixed, the melting point was about 25°C.

実施例 以下に本発明の実施例について説明する。Example Examples of the present invention will be described below.

図に、Na 2 S04−101120およびNa 2
804− ] 0H20とMgSO4・7 I−I20
の混合物の融解曲線を示す。32℃に融点をも−) N
a 2804 @10 T−120にMjj 80.i
 −7I20を混合すると、融解完了温度は図に示す如
(M、9SO4・71−120の混合量と共に低下し、
Na2SO4・10I■201モルに対しM、!9SO
4・7I−I20を07モル混合した試t1では約28
℃で融解が完了する。図に示される様に上記混合物の融
解開始温度は約22℃であり、融解開始と完了の間に約
6℃の温度差が生じ、この温度差はT−1a 2804
−101(zO単独の場合の約2°Cに比べかなり大き
くなる。M、9SO4・7H20の混合量を増加しNa
2SO4・10H20:MgSO4・7H20−1:1
(モル比)の混合物では融解完了温度は約25℃に低下
し、かつ、融解開始と完了の間の温度差も約3°C吉小
さくなる。図では省略しているが、M2SO4・7H2
0の混合量をさらに大きくすると融解完了温度が再び上
昇し、かつ、融解潜熱が次第に低下するのでNa 28
04−101(201モルに対してM、9SO4・7■
I20を15モル以上混合する事は望ましくない。また
、Mg804・7H20の混合量が0.7モル以下にな
ると融解完了温度が28℃以上と高くなりすぎ、また、
融解開始と完了の間の温度差が大きくなりすぎるため、
実用的にはNa2504−10H201モルに対し07
モル乃至15モルのMgSO4・7H205べ−7 を混合する事が望ましい。
The figure shows Na 2 S04-101120 and Na 2
804- ] 0H20 and MgSO4・7 I-I20
The melting curve of the mixture is shown. Melting point at 32℃-)N
a 2804 @10 Mjj 80 on T-120. i
When -7I20 is mixed, the melting completion temperature decreases with the amount of M, 9SO4・71-120 mixed, as shown in the figure.
Na2SO4・10I■M for 201 mole,! 9SO
In test t1, which mixed 07 moles of 4.7I-I20, it was approximately 28
Melting is complete at °C. As shown in the figure, the melting start temperature of the above mixture is about 22°C, and a temperature difference of about 6°C occurs between the start and completion of melting, and this temperature difference is T-1a 2804
-101 (considerably higher than about 2°C in the case of zO alone. By increasing the mixing amount of M, 9SO4・7H20, Na
2SO4・10H20:MgSO4・7H20-1:1
(molar ratio), the melting completion temperature is reduced to about 25°C, and the temperature difference between melting initiation and completion is also about 3°C smaller. Although omitted in the figure, M2SO4・7H2
If the mixing amount of Na 28 is further increased, the melting completion temperature will rise again and the latent heat of fusion will gradually decrease.
04-101 (M for 201 mol, 9SO4・7■
It is not desirable to mix 15 moles or more of I20. Furthermore, if the mixing amount of Mg804.7H20 is less than 0.7 mol, the melting completion temperature will be too high at 28°C or more.
The temperature difference between the start and completion of melting becomes too large;
Practically, 07 per mole of Na2504-10H20
It is desirable to mix mol to 15 mol of MgSO4.7H205b.

なお、この系は非調和融解を示すため、試別の作成には
相分離防止剤として架橋型アクリル酸重合体を2重ff
:%添加し、同時に、過冷却防止剤としてポウ砂を3重
量%添加したが、添加物としてはこれ以外のものでも良
くこれらの添加物の有無は本発明の主旨を逸脱するもの
ではない。
In addition, since this system exhibits anharmonic melting, a cross-linked acrylic acid polymer was used as a phase separation inhibitor to prepare the sample.
:% and at the same time, 3% by weight of porcelain sand was added as an anti-supercooling agent, but other additives may be used and the presence or absence of these additives does not depart from the gist of the present invention.

発明の効果 以上の様に本発明はNa2SO4・10I■20とへ4
1SO4−7H20とを少なくとも含む潜熱蓄熱材を提
供するもので、融解開始を約22℃以」二、融解完了を
約28℃以下に設定する事が可能であり、さらに、本発
明で使用されたNa 2804−107+20 、 M
、t)SO4−7t120はいずれも安価に、かつ、大
量に入手可能な材料であり、毒性もなく不燃性である事
から、本発明による潜熱蓄熱材は電子機器などを設置し
た密閉空間の温度調節用に有用である。
Effects of the Invention As described above, the present invention provides Na2SO4・10I■20 and He4
The present invention provides a latent heat storage material containing at least 1SO4-7H20, which can set the start of melting at about 22°C or lower, and the completion of melting at about 28°C or lower. Na 2804-107+20, M
, t) SO4-7t120 are materials that can be obtained at low cost and in large quantities, and are non-toxic and non-flammable. Therefore, the latent heat storage material according to the present invention can maintain the temperature of the closed space where electronic equipment etc. are installed. Useful for regulation.

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

図は、Na2SO4・10I−120およびNa2SO
4・10■■20とM、9804・10I−I20の混
合物の融解曲線を示す図で6 ページ ある。
The figure shows Na2SO4・10I-120 and Na2SO
There are 6 pages of figures showing the melting curves of mixtures of 4.10■■20 and M, 9804.10I-I20.

Claims (1)

【特許請求の範囲】 1)硫酸ナトリウム10水塩と硫酸マグネシウム7水塩
とを少なくとも含む事を特徴とする潜熱蓄熱材。 2)硫酸ナトリウム10水塩1モルに対し0.7モル及
至1.5モルの硫酸マグネシウム7水塩が混合された事
を特徴とする特許請求の範囲第1項記載の潜熱蓄熱材。
[Claims] 1) A latent heat storage material comprising at least sodium sulfate decahydrate and magnesium sulfate heptahydrate. 2) The latent heat storage material according to claim 1, wherein 0.7 mol to 1.5 mol of magnesium sulfate heptahydrate is mixed with 1 mol of sodium sulfate decahydrate.
JP60220681A 1985-10-03 1985-10-03 Latent heat storage material Expired - Lifetime JPH0641587B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60220681A JPH0641587B2 (en) 1985-10-03 1985-10-03 Latent heat storage material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60220681A JPH0641587B2 (en) 1985-10-03 1985-10-03 Latent heat storage material

Publications (2)

Publication Number Publication Date
JPS6281481A true JPS6281481A (en) 1987-04-14
JPH0641587B2 JPH0641587B2 (en) 1994-06-01

Family

ID=16754799

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60220681A Expired - Lifetime JPH0641587B2 (en) 1985-10-03 1985-10-03 Latent heat storage material

Country Status (1)

Country Link
JP (1) JPH0641587B2 (en)

Also Published As

Publication number Publication date
JPH0641587B2 (en) 1994-06-01

Similar Documents

Publication Publication Date Title
KR840000576B1 (en) Heat or cold storage composition
US5282994A (en) Dry powder mixes comprising phase change materials
KR910000990A (en) Phase Change Materials and Their Uses
JP2005533142A (en) Heat storage medium
JPH0292988A (en) Heat-storing material composition
JPS6281481A (en) Latent heat storing material
JPS6317313B2 (en)
JPS56147884A (en) Regenerating material composition
JPS6251992B2 (en)
JPS6185486A (en) Heat-accumulating material composition
JPS61197668A (en) Thermal energy storage material
JPS58183784A (en) Heat-storing material
JPS60101169A (en) Thermal energy storage material
JPH029707A (en) Antifreezing silicic acid sol
JPS58183785A (en) Heat-storing material
JPS60203689A (en) Thermal energy storage material
JPH1135930A (en) Cold storage material utilizing latent heat
JPH11323320A (en) Latent heat storage agent composition
JPS5941668B2 (en) heat storage material
JPS594677A (en) Cold accumulating material and its preparation
JPS58185680A (en) Heat storage material
JPH1135931A (en) Cold storage material utilizing latent heat
JPS60101168A (en) Thermal energy storage material
JPH0345686A (en) Heat-storage material
GB1004917A (en) Storage block adapted for storage and exchange of heat