JPS6071681A - Heat storage material composition - Google Patents

Heat storage material composition

Info

Publication number
JPS6071681A
JPS6071681A JP17942983A JP17942983A JPS6071681A JP S6071681 A JPS6071681 A JP S6071681A JP 17942983 A JP17942983 A JP 17942983A JP 17942983 A JP17942983 A JP 17942983A JP S6071681 A JPS6071681 A JP S6071681A
Authority
JP
Japan
Prior art keywords
heat storage
storage material
material composition
aluminum silicate
weight
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
JP17942983A
Other languages
Japanese (ja)
Other versions
JPH0417995B2 (en
Inventor
Toshiro Kido
木戸 敏郎
Yutaka Iwamura
岩村 豊
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.)
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Original Assignee
Asahi Chemical Industry Co Ltd
Asahi Kasei 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 Chemical Industry Co Ltd, Asahi Kasei Kogyo KK filed Critical Asahi Chemical Industry Co Ltd
Priority to JP17942983A priority Critical patent/JPS6071681A/en
Publication of JPS6071681A publication Critical patent/JPS6071681A/en
Publication of JPH0417995B2 publication Critical patent/JPH0417995B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a heat storage material composition resistant to the lowering of the quantity of the stored heat by the repetition of melting and freezing, from easily available raw materials, by compounding sodium sulfate decahydrate with hydrated aluminum silicate at a specific ratio. CONSTITUTION:The objective heat storage material composition is produced by compound (A) 100pts.wt. of sodium sulfate decahydrate with (B) 1-20pts.wt. (preferably 4-10pts.wt.) of hydrated aluminum silicate, and if necessary (C) a melting point modifier composed of a eutectic mixture of potassium chloride, aluminum chloride, etc. and (D) a crystal habit modifier composed of preferably sodium laurate, etc.

Description

【発明の詳細な説明】 この発明は、(ビC酸ナトリウム10水塩(Na2SO
a・1oH2O)を主成分とする潜熱蓄熱材組成物にお
いて、融17G−凝固の繰返しによる潜熱蓄熱址の低下
防止技術に関するものである。
DETAILED DESCRIPTION OF THE INVENTION This invention relates to (sodium bicarbonate decahydrate (Na2SO
The present invention relates to a technique for preventing a decrease in the latent heat storage area due to repeated melting and solidification in a latent heat storage material composition containing 17G-17G-solidification as a main component.

従来からNaz80m ・1 oH,oは融解潜熱が5
Q kcal /Kfと大きく、その融点を容易に低下
できるため、例えばヒートボ゛ンプ、ソーラーコレクタ
ー等と組合せた極めて好適な蓄熱材として注目されてい
る。
Conventionally, Naz80m ・1 oH, o has a latent heat of fusion of 5
Since it has a large Q kcal /Kf and its melting point can be easily lowered, it is attracting attention as an extremely suitable heat storage material for use in combination with heat pumps, solar collectors, etc., for example.

しかし、Na2SO4・101420を蓄熱材として使
用する場合には二つの問題がある。その一つは融液を冷
却した際に融点よpも著しく低い温度寸で過冷却する小
である。この過冷却現象は放熱を行う場合、相変化時の
融解潜熱を放出せずに液として温度が低下するため蓄熱
材としては致命的な欠点となる、この過冷却現象を防止
する手段としては、核生成物質として四ホウ酸ナトリウ
ム10水塩(Na2B407 ・10H20) fr、
添加することで解決される事が米国特許2667664
号明細書に開示されておシ、本発明の組成物でもこの過
冷却防止に、Na2B4O7・10H20等を使用する
事は前提としている。
However, there are two problems when using Na2SO4.101420 as a heat storage material. One of them is that when the melt is cooled, it is supercooled at a temperature significantly lower than the melting point. This supercooling phenomenon is a fatal drawback for heat storage materials because when heat is dissipated, the temperature drops as a liquid without releasing the latent heat of fusion during phase change.As a means to prevent this supercooling phenomenon, As a nucleating substance, sodium tetraborate decahydrate (Na2B407 ・10H20) fr,
U.S. Patent No. 2,667,664 shows that the problem can be solved by adding
The composition of the present invention as disclosed in the specification of the present invention is also based on the premise that Na2B4O7.10H20 or the like is used to prevent supercooling.

他一つの問題はNa2SO4・1oH,Oの融解特性が
非調和を示す事である。すなわちN a 2 S O4
・10 H2Oは融解時にNa2SO4飽和溶液とN 
a 2 S 04の固体の2相に分離し、Na2SO4
の固体は溶液に比べて密度が太きいために容器の底に沈
頗する。
Another problem is that the melting properties of Na2SO4.1oH,O are anharmonic. That is, N a 2 S O4
・10 H2O mixes with Na2SO4 saturated solution and N when melted.
Separates into two solid phases of a2S04, Na2SO4
Since the solid is denser than the solution, it settles to the bottom of the container.

この2相に分離した系を冷却するとまず沈υしたN a
 2 S O4の上部にNa2SO4の結晶が形成され
障壁となって残シのNa2SO4がH2Oと結合してN
a2SO4+10H,Oの結晶になる事を妨げる。この
だめ残留したNa2SO4は相変化に寄与しなくなシ潜
熱蓄熱量が大幅に低下する問題がある。
When the system separated into two phases is cooled, firstly the precipitated Na
2 Na2SO4 crystals are formed on top of SO4 and act as a barrier, and the remaining Na2SO4 combines with H2O and N
Prevents crystallization of a2SO4+10H,O. There is a problem that the remaining Na2SO4 no longer contributes to the phase change and the amount of latent heat stored is significantly reduced.

実用に際して最も重要な上記の相分離の問題を解決する
ために、融解時の液をゲル化し、固体のN a 2 S
 O4の沈澱を防ぎ、均一に分散懸濁きせる方法が提案
されている。
In order to solve the above-mentioned problem of phase separation, which is most important in practical use, the molten liquid is turned into a gel, and the solid Na 2 S
A method has been proposed that prevents precipitation of O4 and allows it to be uniformly dispersed and suspended.

具体的には相分離防止材に、おがくず、・ξルプメチル
セルロール、シリカゲル、各種粘土等を用いる方法があ
り、その中でもアタノξルジャイト粘土が好適である事
が特開昭53−34687号公報に記載されている。し
かしながら上記アタ・ξルジャイト粘土を含む組成物の
蓄熱材は融解−凝固の繰返しによる蓄熱量の劣下は避は
短く、例えば、300回の融解−凝固の繰返しサイクル
ですでに蓄熱量が約30 kcal /に9に低下して
しまう等の問題がある。又、アタパルジイト粘土は輸入
品であることから入手が困難という問題もある。上述し
たように、Na2SO4・10)120の相分離現象に
対する防止策には問題点が多く、実用比のためには入手
が容易でしかも蓄熱量の劣化の低減した蓄熱材組成物が
要望されている。
Specifically, there are methods of using sawdust, ξulpmethylcellulose, silica gel, various clays, etc. as phase separation prevention materials, and among these methods, JP-A-53-34687 discloses that athano-ξlugite clay is suitable. It is described in. However, in the heat storage material of the composition containing the above-mentioned atta-ξurgite clay, the deterioration of the heat storage amount due to repeated melting and solidification is short-lived; for example, after 300 melting and solidification cycles, the heat storage amount has already reached approximately 30 There are problems such as the kcal / drop to 9. Furthermore, since attapulgite clay is an imported product, there is also the problem that it is difficult to obtain. As mentioned above, there are many problems in preventing the phase separation phenomenon of Na2SO4.10)120, and for practical use, there is a need for a heat storage material composition that is easy to obtain and has reduced deterioration in heat storage amount. There is.

本発明はこのような現状に鑑みてなされたもので、その
目的は、入手が容易なゲル化材で相分離を防止し、融解
潜熱をより有効に利用できしかも融解−凝固の繰返しに
対して十分な能力を保持する蓄熱量を提供する小にある
The present invention was made in view of the current situation, and its purpose is to prevent phase separation using an easily available gelling material, to utilize the latent heat of fusion more effectively, and to prevent repeated melting and solidification. It has a small capacity to provide sufficient heat storage capacity.

上記目的は、Na2’SOa・101(20を主成分と
する潜熱蓄熱材組成物において、Na2SO4・101
−120,100重量部に対して、水和ケイ酸アルミニ
ウム1〜20重Hj′L部全含有している組成物を利用
する事によって容易に達成される。
The above purpose is to prepare a latent heat storage material composition containing Na2'SOa.101 (20) as a main component.
This can be easily achieved by using a composition containing 1 to 20 parts by weight of hydrated aluminum silicate to 120,100 parts by weight.

本発明の主友部は相分離防止材として、水和ケイ唆アル
ミニウムを用いる事にある。
The main feature of the present invention is the use of hydrated silicon-induced aluminum as a phase separation preventing material.

N a 2 S O4・10 H□0に水和ケイl”1
Mアルミニウムを少量添加すると、著しく水和して安定
なゲルを生成し、Na2SO4・IOH,Oの粒子の沈
降を防止し、相分離防止効果の役割をするもので1部以
上必要である。
N a 2 S O4・10 H□0 to hydrated silica l”1
When M aluminum is added in a small amount, it is significantly hydrated to form a stable gel, which prevents sedimentation of Na2SO4.IOH,O particles and plays a role in preventing phase separation, and 1 part or more is required.

副加量はNa2SO4” 10 I20 、100重量
部に対して、20重量部を越えて多い場合には重量当り
の潜熱量が低下し、しかも溶液粘度が高く攪拌調合が難
かしくなる。
If the sub-addition exceeds 20 parts by weight per 100 parts by weight of Na2SO4"10 I20, the amount of latent heat per weight decreases, and the solution viscosity becomes high, making stirring and preparation difficult.

従って本発明でいう蓄熱材組成では水和ケイ酸アルミニ
ウムを1〜20重量部宮有することが必要で相分離防止
効果及び単位重量当りの蓄熱量の点から効果的には4〜
10重量部を選ぶ事が望寸しい。
Therefore, in the heat storage material composition of the present invention, it is necessary to have 1 to 20 parts by weight of hydrated aluminum silicate, and from the viewpoint of phase separation prevention effect and heat storage amount per unit weight, it is necessary to have 4 to 20 parts by weight of hydrated aluminum silicate.
It is desirable to select 10 parts by weight.

水利ケイ酸アルミニウムとは一般的に化孝式では、At
2Si401o(OH)2− nH2Oで表わさすし、
代表的には例えば商品名オスモスNの呼称で、白石工づ
、=(株)から重版されておシ答易に入手できる拐料で
ある。
Irrigation aluminum silicate is generally known as At
It is expressed as 2Si401o(OH)2-nH2O,
Typically, it is a reprinted product from Shiraishi Kozu Co., Ltd., which is easily available under the trade name Osmos N.

本発明の蓄熱材組成物には公知の融点調整材、例えば、
塩化カリウム、塩化アルミニウム、塩化ナトリウム、硝
酸カリウム等の共融物においても相分離防止材として使
用可能である。象に晶癖変調材、例えば、ヘキサメタリ
ン駿ソーダ、オレイン酸ソーダ、ラウリン酸ソーダ等を
添加して使用することも可能であり特に効果的には、ラ
ウリン酸ソーダとの組合せが好すしい。
The heat storage material composition of the present invention may include known melting point adjusting materials, such as
Eutectic compounds of potassium chloride, aluminum chloride, sodium chloride, potassium nitrate, etc. can also be used as phase separation preventive materials. It is also possible to use crystal habit modifiers, such as sodium hexamethaline, sodium oleate, sodium laurate, etc., added to the crystal, and the combination with sodium laurate is particularly effective.

以下、実施pH、比較例によってその内容を明らかにす
る。
The details will be clarified below with reference to the working pH and comparative examples.

実施例、比較例−1 N a 2804 ・10 I20 、100重量部に
対して、Na2B4O7”10)I20を3重量部と水
和クイ酸アルミニウムを各々1,7.20爪量部を加え
3種類の試料L1ぎし順次■■■と付した。
Examples, Comparative Examples-1 To 100 parts by weight of Na 2804 10 I20, 3 parts by weight of Na2B4O7''10) I20 and 1 and 7.20 parts of hydrated aluminum citrate were added to 3 types. The sample L1 was marked with ■■■.

別に比佼試料として、上記の水和ケイ酸アルξニウムの
ないものと、水和ケイ酸アルミニウムの代りにアタ・々
ル)Yイト粘土を7 p+、 、’LH(部加えたもの
ケ順次代4′A番号を■、■と付した。
Separately, as samples, the above-mentioned one without hydrated aluminum silicate, and the one with 7 p+, , 'LH (parts added) in place of hydrated aluminum silicate. The 4'A numbers are marked ■ and ■.

これら5種類の試料に付き、初期潜熱値の測定と融解−
凝固を100 、200 、300ザイクル^、7÷返
した陵の71に熱蓄熱量とを測定しその値を表−1に示
した。
Measurement of initial latent heat values and melting of these five types of samples -
The heat storage amount was measured for 100, 200, and 300 cycles of solidification, 7 divided by 71, and the values are shown in Table 1.

尚、熱量測定は差動熱Xi−計を用いて6111定した
Incidentally, the calorific value was measured using a differential heat Xi-meter.

上記融町−凝固の1サイクルは60℃(完全融解)から
、0℃(完全凝固)の状態を1サイクルとして、1サイ
クルに6時間を快しで行うようにして評価した。
One cycle of the melting process described above was performed from 60° C. (complete melting) to 0° C. (complete solidifying), and the evaluation was carried out for 6 hours per cycle.

表−1から次の哄が明らかである。From Table-1, the following song is clear.

初期値から300サイクル捷での7’tT熱の低下は試
料番号■が7、■が3、■が2、■が45、■が11 
kcal /にりとなっておシ、水利ケイ酸アルミニウ
ムがアク・ξルジャイト粘土より相分離防止効果が大き
いことがわかる。
The decrease in 7'tT heat after 300 cycles from the initial value is 7 for sample number ■, 3 for ■, 2 for ■, 45 for ■, and 11 for ■.
It can be seen that the water-use aluminum silicate has a greater effect of preventing phase separation than the aqueous ξurgite clay.

又、試料番号■と■の対比より、添加量がアタ/ξルジ
ャイト粘土が7重量部と水利ケイ酸アルミニウムが20
重量部のときの初期潜熱量がほぼ同じで、添加量を増大
させることで繰返し安定性が向上する利点の生じること
が示きれている。
Also, from the comparison between sample numbers ■ and ■, the amount added is 7 parts by weight of Ata/ξ Lugite clay and 20 parts by weight of aluminum silicate.
It has been shown that the initial latent heat amount in parts by weight is almost the same, and that increasing the amount added has the advantage of improving repeat stability.

本発明は上述の構成を持つ事により、融解潜熱をより有
効に利用でき、入手容易々相分p:1「防止材を月4い
て、しかも繰返し安定性の優れた蓄熱材組成物を提供す
ることができる。
By having the above-mentioned structure, the present invention provides a heat storage material composition that can utilize the latent heat of fusion more effectively, is easily available, contains a phase ratio of P:1, and has excellent cyclic stability. be able to.

又、本発明の蓄熱材組成物を使用する事により今後一段
と重要視される熱エネルギーの有効利用に貢献するもの
である。
Furthermore, the use of the heat storage material composition of the present invention contributes to the effective use of thermal energy, which will become more important in the future.

特許出願人 旭化成工業株式会社Patent applicant: Asahi Kasei Industries, Ltd.

Claims (1)

【特許請求の範囲】[Claims] 硫酸ナトリウム10水塩を主成分とする潜熱蓄熱材組成
において硫覆ナトリウム10水塩100重量部に対して
、水和ケイ酸アルミニウムを1〜20重量部官有してい
ることを特徴とする潜熱蓄熱材組成物
A latent heat storage material composition containing sodium sulfate decahydrate as a main component, which contains 1 to 20 parts by weight of hydrated aluminum silicate per 100 parts by weight of sodium sulfate decahydrate. Heat storage material composition
JP17942983A 1983-09-29 1983-09-29 Heat storage material composition Granted JPS6071681A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17942983A JPS6071681A (en) 1983-09-29 1983-09-29 Heat storage material composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17942983A JPS6071681A (en) 1983-09-29 1983-09-29 Heat storage material composition

Publications (2)

Publication Number Publication Date
JPS6071681A true JPS6071681A (en) 1985-04-23
JPH0417995B2 JPH0417995B2 (en) 1992-03-26

Family

ID=16065699

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17942983A Granted JPS6071681A (en) 1983-09-29 1983-09-29 Heat storage material composition

Country Status (1)

Country Link
JP (1) JPS6071681A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008093876A1 (en) * 2007-01-31 2008-08-07 Showa Kde Co., Ltd. Latent-heat storage material composition and process for producing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008093876A1 (en) * 2007-01-31 2008-08-07 Showa Kde Co., Ltd. Latent-heat storage material composition and process for producing the same
JP2008184589A (en) * 2007-01-31 2008-08-14 Showa Kde Co Ltd Latent heat storage material composition and its manufacturing method

Also Published As

Publication number Publication date
JPH0417995B2 (en) 1992-03-26

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