JPS59187076A - Heat accumulative material - Google Patents

Heat accumulative material

Info

Publication number
JPS59187076A
JPS59187076A JP58060131A JP6013183A JPS59187076A JP S59187076 A JPS59187076 A JP S59187076A JP 58060131 A JP58060131 A JP 58060131A JP 6013183 A JP6013183 A JP 6013183A JP S59187076 A JPS59187076 A JP S59187076A
Authority
JP
Japan
Prior art keywords
hydrate
sodium
heat storage
storage material
sodium sulfite
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
JP58060131A
Other languages
Japanese (ja)
Inventor
Yasuo Kudo
康夫 工藤
Takeshi Takeda
竹田 武司
Ikuhiko Machida
町田 育彦
Kazutoshi Iketani
池谷 和俊
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 JP58060131A priority Critical patent/JPS59187076A/en
Publication of JPS59187076A publication Critical patent/JPS59187076A/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
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/40Solar thermal energy, e.g. solar towers

Abstract

PURPOSE:A heat accumulative material for heating of passive solar house, hothouse, etc., obtained by adding sodium sulfite.7 hydrate or anhydride to a system containing sodium sulfate.10 hydrate and sodium carbonate.10 hydrate. CONSTITUTION:A system containing sodium sulfate.10 hydrate and sodium carbonate.10 hydrate in a molar ratio of preferably (5:4)-(1:2) is blended with at least one of sodium sulfite.7 hydrate or sodium sulfite anhydride in a molar ratio of preferably (0.95:0.05)-(0.85:0.15), to give the desired heat accumulative material.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は主としてパッシブソーラーノ・ウスの暖房や温
室の暖房等に用いられる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 primarily to a heat storage material used for passive solar heating, greenhouse heating, and the like.

従来例の構成とその問題点 冬期に、昼間の太陽熱を貯蔵しこれを夜間の暖房に利用
するいわゆるパノシブンーラ暖房システムに使用される
潜熱蓄熱材としては、硫酸ナトリウム10水塩(Na2
SO4・10H20)や塩化カルンウム6水塩(CaC
12・6H20)がよく知られている。前者は約32℃
、後者は約29°Cに融点を持ち、パンシブンーラ暖房
システムに使用できるとは云うものの、より汎用性をも
たせるためには融点を20乃至26℃に低下せしめる事
が望まれていた。本発明者らは、先行出願において、約
24℃に融点をもつ新規な蓄熱材、すなわち、Na2S
O4・1oH2oとNa2CO3・1oH20の共融混
合物を開示したが、この先行出願における蓄熱材の施設
園芸(ビニルノ・ウス)への適用を検討した結果、融点
をさらに低下させ20’Cに近づける事が望ましいとの
結論を得た。
Conventional configuration and its problems During the winter, sodium sulfate decahydrate (Na2
SO4・10H20) and carunium chloride hexahydrate (CaC
12.6H20) is well known. The former is about 32℃
Although the latter has a melting point of about 29°C and can be used in the Pansibunula heating system, it has been desired to lower the melting point to 20 to 26°C in order to make it more versatile. In a previous application, the present inventors have proposed a novel heat storage material with a melting point of about 24°C, namely Na2S.
Although a eutectic mixture of O4.1oH2o and Na2CO3.1oH20 was disclosed, as a result of considering the application of the heat storage material to greenhouse horticulture (vinyl gardening) in this earlier application, it was found that the melting point could be further lowered to approach 20'C. The conclusion was that it is desirable.

発明の目的 本発明は上記の事情に鑑みて、前記 Na2SO4・1QH20とNa2CO3@10H20
の共融混合物から成る蓄熱材の融点をさらに低下せしめ
るためになされたものである。
Purpose of the Invention In view of the above circumstances, the present invention provides the above-mentioned Na2SO4.1QH20 and Na2CO3@10H20.
This was done in order to further lower the melting point of a heat storage material made of a eutectic mixture of

発明の構成 本発明の蓄熱材はNa2 SO4・10H20とNa 
2CO3・1oH20を少なくとも含み、さらに亜硫酸
ナトリウム7水塩(Na2S○3・”’rH20)−4
たけ亜硫酸ナトリウム無水物(Na2sO3)を添加し
て得られる。本発明の特徴は1(a2 SO4・10H
20とNa2CO3・1QH20を主成分とした蓄熱材
の融点をMa2SO3・7H20もしくはNa2SO3
を添加することによりさらに低下せしめたことにある。
Structure of the Invention The heat storage material of the present invention includes Na2SO4・10H20 and Na
Contains at least 2CO3・1oH20, and further contains sodium sulfite heptahydrate (Na2S○3・”'rH20)-4
Obtained by adding bamboo shoot sodium sulfite anhydride (Na2sO3). The characteristics of the present invention are 1 (a2 SO4・10H
The melting point of the heat storage material whose main components are 20 and Na2CO3・1QH20 is Ma2SO3・7H20 or Na2SO3
This was further reduced by adding .

前記Na 2 SOs・7H20は実質的に含まれてい
ればよく、Na2SO3・7H2Qをそのま1単独で用
いるほか、Na 2 SOsおよびその7水塩を生成す
るのに必要な化学量論量の水の両者を用いることもでき
る。
It is sufficient that the Na 2 SOs 7H20 is substantially contained, and in addition to using Na2SO3 7H2Q alone as it is, a stoichiometric amount of water necessary to generate Na 2 SOs and its heptahydrate is used. It is also possible to use both.

また、この他に過冷却抑制のだめの核生成剤や特性改善
のためのゲル化剤や界面活性剤等の混合の有無は、本発
明の基本的構成を変えるものでなく、本発明の主旨を逸
脱するものではない。
In addition, the presence or absence of a nucleating agent to suppress supercooling, a gelling agent, a surfactant, etc. to improve properties does not change the basic structure of the present invention, and does not affect the gist of the present invention. It's not something to deviate from.

実施例の説明 〈実施例1〉 Na25o4・1QH20とNa2CO3・10馬Oと
Na2SO3・7H20とをモル比で(1−x ) /
 2 :(1−x )/2 : xの割合で混合し、x
 −0,05。
Description of Examples <Example 1> Na25o4.1QH20, Na2CO3.10H20 and Na2SO3.7H20 in molar ratio (1-x)/
2: (1-x)/2: Mix at a ratio of x, x
-0,05.

0.10,0.15,0.20の4種の試料を作製した
Four types of samples of 0.10, 0.15, and 0.20 were prepared.

試料は過冷却防止剤として3重H%のホウ砂(Na2B
407・1oH2Q)、相分離防止剤として2重量%の
架橋型アクリル酸重合体を含んでいるが、これらは試H
の融点に殆んど影響しない事が確認された。これらの試
料を約3oi密閉型ポリエチレン容器に入れ、温度測定
用の熱電対を試料の中心部に挿入し、融解、凝固の温度
プロフィルを測定し、先行出願におけるNa25o3・
7 H2Oを含まないX=Oのそれと比較した。図に示
された様に、x−oの試料を10℃の水槽の中で完全に
凝固させ、ついで30℃の水槽中で融解させた場合試料
温度約23℃から融解が始まり、約24.6℃で融解が
完了した。
The sample contained 3% H borax (Na2B) as an anti-supercooling agent.
407・1oH2Q), which contains 2% by weight of crosslinked acrylic acid polymer as a phase separation inhibitor, but these
It was confirmed that it had almost no effect on the melting point of These samples were placed in an approximately 3 oi sealed polyethylene container, a thermocouple for temperature measurement was inserted into the center of the sample, and the temperature profile of melting and solidification was measured.
7 Compared with that of X=O which does not contain H2O. As shown in the figure, when the x-o sample was completely solidified in a water bath at 10°C and then melted in a water bath at 30°C, melting started at a sample temperature of about 23°C, and melting started at about 24°C. Thawing was complete at 6°C.

X=0.05の試料では融解開始温度が約22℃。The melting start temperature for the sample with X=0.05 is approximately 22°C.

融解完了温度が約23.5’C、yc−0,1の試料で
は前者約21−5’C; +後者約23”0.、x−0
,16の試料では前者約21.5’C,後者約23.5
℃、またX=0・2の試料では前者約20’C,後者約
24℃と、両者共像下が見られた。ただXの増加と共に
融解開始温度と完了温度の差が大きくなる傾向に加えて
、融解開始から完了までに要する時間がケ豆くなる傾向
が認められ、これらの傾向はX二0.2の試料において
顕著である。後者の傾向は蓄熱量の低下を示しており、
したがってXの範囲としては、0.06乃至0.16が
望ましく、特に望ましい範囲は0.05乃至0.1であ
る。
The melting completion temperature is about 23.5'C, for the sample yc-0,1 the former is about 21-5'C; + the latter is about 23"0., x-0
, 16 samples, the former is about 21.5'C and the latter is about 23.5'C.
℃, and for the sample with X=0.2, the former was approximately 20'C and the latter was approximately 24°C, both of which were observed to be under the same image. However, as X increases, the difference between melting start temperature and melting completion temperature tends to increase, and the time required from melting start to completion tends to decrease. It is noticeable in The latter trend indicates a decrease in heat storage,
Therefore, the range of X is preferably 0.06 to 0.16, and a particularly desirable range is 0.05 to 0.1.

〈実施例2〉 Na25O4e10H20とNa2CO3弓0H2oと
Na2SO3・7H2oをモル比テy : (0−9−
y ) :0.1の割合で混合し、y=0.55,0.
50,0.45゜0.40,0.35,0.30,0.
25の7種の試料を作成した。過冷却防止剤、相分離防
止剤は実施例1におけると同様に添加された。7=0.
45の試料は、実施例1におけるX−〇、10の試料と
同一のものであり、yが0.60乃至0.30の範囲に
ある試料の融解曲線は、y=0.45のそれと大差なか
ったが、yが0.55,0.25の試料の融解曲線では
かなりの変化がみられ、22乃至23℃に融点をもつ相
似外に、27乃至28℃に融点をもつ相の出現がみとめ
られ、本発明の目的に適さない事が判明した。従って、
Na 2 SO4・i o H2OとNa2CO3−1
0H20のモル数の和に対し、Na 2SO3・7H2
0のモル比がo、iの場合yの範囲は0.50乃至0.
30.すなわち、Na2SO4・10H2゜トNa2C
O3−1QH20はモ/lz比で0.50:0.40乃
至0.30:o、eoの割合で含まれる事が望ましい。
<Example 2> Molar ratio of Na25O4e10H20, Na2CO3 0H2o and Na2SO3・7H2o: (0-9-
y): mixed at a ratio of 0.1, y=0.55, 0.
50, 0.45° 0.40, 0.35, 0.30, 0.
25 seven types of samples were prepared. The supercooling inhibitor and phase separation inhibitor were added in the same manner as in Example 1. 7=0.
Sample No. 45 is the same as sample X-○ and No. 10 in Example 1, and the melting curves of the samples with y in the range of 0.60 to 0.30 are significantly different from those with y = 0.45. However, considerable changes were observed in the melting curves of samples with y of 0.55 and 0.25, and in addition to the similar phase with a melting point between 22 and 23 degrees Celsius, a phase with a melting point between 27 and 28 degrees Celsius appeared. It was found to be unsuitable for the purposes of the present invention. Therefore,
Na2SO4・io H2O and Na2CO3-1
For the sum of moles of 0H20, Na2SO3・7H2
When the molar ratio of 0 is o, i, the range of y is 0.50 to 0.
30. That is, Na2SO4・10H2°tNa2C
It is desirable that O3-1QH20 be contained in a mo/lz ratio of 0.50:0.40 to 0.30:o, eo.

またNa2SO4・1oH20とNa2cO3・1oH
2Q のモル数の和に対し、Na2SO3・7)(20
のモ/l/数がo、95:0.05乃至o、aes:o
、16の範囲になる様にNa2SO3・7H20を加え
た場合でも、前記の範囲、すなわちNa2SO4・10
H20とNa2CO3・10H20の0.33)ニー(
=0.67)の範囲にあれば、273 乃至28゛Cに融点を持つ相は観測されず、望ましい特
性を示した。
Also, Na2SO4・1oH20 and Na2cO3・1oH
For the sum of moles of 2Q, Na2SO3・7)(20
Mo/l/number is o, 95:0.05 to o, aes:o
, 16, even if Na2SO3.7H20 is added to the range of 16, the above range, that is, Na2SO4.10
H20 and Na2CO3・10H20 0.33) Knee (
= 0.67), no phase with a melting point between 273°C and 28°C was observed, indicating desirable properties.

〈実施例3〉 N2SO3・7H2o7)代わりにNa2SO3を用い
た以外実施例1と同様に試料を作製し、測定を行なった
ところ実施例1とほぼ同様の結果が得られた。
<Example 3> A sample was prepared in the same manner as in Example 1 except that Na2SO3 was used instead of N2SO3.7H2o7), and measurements were performed, and almost the same results as in Example 1 were obtained.

なお本発明者らは先行出願において、硫酸ナトリウム1
o水塩と炭酸ナトリウム1o水塩を主成分とし融点を低
下させるため、さらに塩化ナトリウム、塩化カリウムの
うち少なくとも1種もしくは尿素を含む蓄熱材を開示し
たが、これらの先行出願による発明と本発明を組み合わ
せた場合においても融点を低下せしめる効果が同様に得
られることはもちろんである。
In addition, the present inventors have reported in the earlier application that sodium sulfate 1
Although a heat storage material which is mainly composed of o hydrate and sodium carbonate hydrate and further contains at least one of sodium chloride, potassium chloride, or urea in order to lower the melting point, the invention based on these earlier applications and the present invention It goes without saying that the same effect of lowering the melting point can be obtained even when these are combined.

発明の効果 以上述べたように、本発明は硫酸ナトリウム10水塩と
炭酸ナトリウム10水塩を少なくとも含む蓄熱材に亜硫
酸す) IJウム了水塩捷たは亜硫酸ナトリウム無水物
のうち少くとも一方を添加し融点を低下せしめ、20″
Cに近づけるようにしたものであり、本発明による蓄熱
材はパソシプンーラー暖房ンステム、中就施設園芸の暖
房システムに特に有用である。
Effects of the Invention As described above, the present invention provides a heat storage material containing at least sodium sulfate decahydrate and sodium carbonate decahydrate, and at least one of sodium sulfite decahydrate and sodium sulfite anhydrous. Added to lower the melting point, 20″
The heat storage material according to the present invention is particularly useful for heating systems for pasocipunlar heating systems and greenhouse horticulture.

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

図は、本発明による蓄熱材の融解曲線の例を示す図であ
る。
The figure is a diagram showing an example of a melting curve of a heat storage material according to the present invention.

Claims (1)

【特許請求の範囲】 (リ 硫酸ナトリウム1o水塩と炭酸ナトリウム1o水
塩を少なくとも含み、さらに亜硫酸ナトリウム7水塩ま
たは亜硫酸ナトリウム無水物の少くともいずれか一方を
添加したことを特徴とする蓄熱材。 (2)硫酸ナトリウム10水塩と炭酸ナトリウム1o水
塩のモル数の和に対する亜硫酸ナトリウム7水塩もしく
は亜硫酸ナトリウム無水物のいずれか一方のモル数また
はモル数の和の比率が0.96=0.05乃至0.85
:0.15の範囲にあることを特徴とする特許請求の範
囲第1項記載の蓄熱材。 (3)硫酸ナトリウム1o水塩と炭酸ナトリウム1o水
塩のモル比が6=4乃至1:2の範囲にあることを特徴
とする特許請求の範囲第1項記載の蓄熱材。
[Scope of Claims] (A heat storage material characterized by containing at least sodium sulfate monohydrate and sodium carbonate monohydrate, and further adding at least one of sodium sulfite heptahydrate or sodium sulfite anhydride. (2) The ratio of the number of moles or the sum of the number of moles of either sodium sulfite heptahydrate or sodium sulfite anhydride to the sum of the number of moles of sodium sulfate decahydrate and sodium carbonate monohydrate is 0.96 = 0.05 to 0.85
:0.15. (3) The heat storage material according to claim 1, wherein the molar ratio of sodium sulfate 1O hydrate to sodium carbonate 1O hydrate is in the range of 6=4 to 1:2.
JP58060131A 1983-04-06 1983-04-06 Heat accumulative material Pending JPS59187076A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58060131A JPS59187076A (en) 1983-04-06 1983-04-06 Heat accumulative material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58060131A JPS59187076A (en) 1983-04-06 1983-04-06 Heat accumulative material

Publications (1)

Publication Number Publication Date
JPS59187076A true JPS59187076A (en) 1984-10-24

Family

ID=13133269

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58060131A Pending JPS59187076A (en) 1983-04-06 1983-04-06 Heat accumulative material

Country Status (1)

Country Link
JP (1) JPS59187076A (en)

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