JPS582598A - Heat accumulating material - Google Patents

Heat accumulating material

Info

Publication number
JPS582598A
JPS582598A JP10181681A JP10181681A JPS582598A JP S582598 A JPS582598 A JP S582598A JP 10181681 A JP10181681 A JP 10181681A JP 10181681 A JP10181681 A JP 10181681A JP S582598 A JPS582598 A JP S582598A
Authority
JP
Japan
Prior art keywords
heat accumulating
accumulating material
nucleator
heat storage
added
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
JP10181681A
Other languages
Japanese (ja)
Inventor
Kazuo Nomura
一夫 野村
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 Electric Works Co Ltd
Original Assignee
Matsushita Electric Works 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 Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP10181681A priority Critical patent/JPS582598A/en
Publication of JPS582598A publication Critical patent/JPS582598A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K5/00Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
    • C09K5/02Materials undergoing a change of physical state when used
    • C09K5/06Materials undergoing a change of physical state when used the change of state being from liquid to solid or vice versa
    • C09K5/063Materials absorbing or liberating heat during crystallisation; Heat storage materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Combustion & Propulsion (AREA)
  • Thermal Sciences (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)

Abstract

PURPOSE:To prevent supercooling of a heat accumulating material, by adding brium acetate to a heat accumulating material of CaCl2.6H2O as a nucleator for preventing supercooling of the heat accumulating material. CONSTITUTION:Barium acetate is added to CaCl2.6H2O as a nucleator for preventing supercooling. Although the nucleator is added at a rate higher than the solubility of the same, it is practically preferable that the amount of the nucleator to be added to CaCl2.6H2O is less than 10wt% of CaCl.6H2O. A thickening agent can be added further to CaCl2.6H2O for the purpose of improving diffusion of the nucleator. As the thickening agent, a high-molecular substance such as carboxymethylcellulose that is dissolved in a heat accumulating material is used. Resultantly, it is enabled to obtain a heat accumulating material capable of preventing supercooling and having a stable performance, absorbing and releasing heat at a fixed temperature.

Description

【発明の詳細な説明】 +1)  発明の目的 過冷却を防止した蓄熱材を提供することt−目的とする
[Detailed Description of the Invention] +1) Object of the Invention It is an object of the invention to provide a heat storage material that prevents supercooling.

t2)従来例 蓄熱方式は大きく分けると、−熱利用方式、潜熱利用方
式、化学蓄熱方式の3種かめる。*熱蓄熱は水や砂など
の顕熱を利用するもので、一般に広く用いられているも
のである。しかし、このタブプは、蓄熱容量が小さい木
め、装置が大きくなってし!う、化学蓄熱は反応熱や希
釈熱を利用するものであるが、このタイプのものは反応
が関与するため制御がむずかしく、装置が複雑になる。
t2) Conventional Example Heat storage methods can be roughly divided into three types: - heat utilization method, latent heat utilization method, and chemical heat storage method. *Thermal storage uses the sensible heat of water, sand, etc., and is widely used. However, this tabpu is made of wood, which has a small heat storage capacity, and the device is large! Chemical heat storage uses reaction heat and dilution heat, but this type of heat storage involves reactions, making it difficult to control and requiring complicated equipment.

これ一対し、sm&蓄熱は、蓄熱容量が大@vs九め、
装置の1コンパクト化が可能、下あり%また複IIaな
装置も必要としない龜 潜熱臘蓄熱材としては、蓄熱賽量が大重いことなどから
、無機水和物牟有、望ζ思わ乃±が1.こめ無機水和物
には過冷却という問題がある。すなわち、冷却すると溶
融状−からl!fil1.その−凝固熱か出るのか一般
的であるが、無機水和物では冷却しても、しばしば凝m
<ず、#−状膳の筐\であることが多い、これが過冷却
構象て、この′kA象が起こnば、凝固熱がとや出せず
、従って、蓄熱材としての意味かなくなる。
On the other hand, SM & heat storage has a large heat storage capacity @vs.
As a latent heat storage material, it is possible to make the device more compact, and it does not require a multi-layered device.Since the amount of heat storage is very heavy, inorganic hydrates and other materials are preferable. is 1. Rice inorganic hydrates have the problem of supercooling. That is, when cooled, it changes from a molten state to l! fil1. Generally speaking, inorganic hydrates often produce coagulation heat even when cooled.
This is often a #-shaped box, which is a supercooled structure, and if this ``kA phenomenon'' occurs, it will not be able to release much solidification heat, and therefore it will be useless as a heat storage material.

無機蓄熱材として塩イ【カルシウム六水塩(CaC1r
15HsO)が知らnているが、このものも上記欠点を
有して艷たのである。。
Salt [calcium hexahydrate (CaC1r)] is used as an inorganic heat storage material.
15HsO) is known, but this one also had the above-mentioned drawbacks and was rejected. .

(3)発明の構成 本発明は、塩化カルシクム六水塩中に、過冷却防止用の
核剤として酢酸バリウムを添加してなる蓄熱材を提供す
るものである。
(3) Structure of the Invention The present invention provides a heat storage material made by adding barium acetate as a nucleating agent for preventing supercooling to calcium chloride hexahydrate.

塩化カルシウム六水塩(Caclm・@HsO]は一点
が2*Cで75cal/−の大きな融解漕熱を有する。
Calcium chloride hexahydrate (Caclm@HsO) has a large melting vessel heat of 75 cal/- at 2*C.

しかしCaclm・(lHsoは、oc以下まで容易に
過冷却し、との筐\では蓄熱材として使用できない、そ
こで上記の1うな核剤t、sm度以上に加える。・する
と綱体として存在する核剤がCaclm・6出0の結晶
化が始まる。結晶化の過程は、液体から固体の析出する
結晶核と生成過程と、一体である結晶の成長過程に分け
らnる。
However, Caclm (lHso) is easily supercooled to below oc and cannot be used as a heat storage material in a case of .Therefore, the above-mentioned nucleating agent is added above t and sm degrees. Crystallization of the agent Caclm.6 out0 begins. The crystallization process is divided into a crystal nucleus and generation process in which a solid is precipitated from a liquid, and a crystal growth process which is an integrated process.

結晶核の発生は、非平衝状−におけるユラギの現象とし
て統計的に扱われるが、モデル的には、少数op子団で
構成される結晶核のかけらともいうべき胚珠か溶液から
生成し、それか成長して結晶核となる通機として捉えら
れる。こ\で結晶核はバルクの鰯蟲の構成粒子(分子、
原子、イすン等)が少なくと4単位格子の数倍以上系っ
て購則正しい配列tとったもの\如(考えられる。胚珠
は臨界結晶砿牛嫌より大11なtのになると成長して、
この結l1lI核となるが、Caclm;61110は
胚珠が臨界結晶値亭径以上の大きさになる時のエネルギ
ーギャップが大きいため、蓄しい過冷却を示すものと思
われる。そして核剤はこのエネルギーギャップを小さく
する役割をしているものと考えられる。
The generation of a crystal nucleus is treated statistically as a phenomenon of fluctuation in a non-equilibrium state, but in terms of a model, it is generated from an ovule or a solution, which can be called a fragment of a crystal nucleus composed of a small number of opiates. Otherwise, it can be seen as a through-hole that grows and becomes a crystal nucleus. Here, the crystal nuclei are the constituent particles (molecules,
It is conceivable that the number of atoms (atoms, atoms, etc.) is at least several times as large as the 4 unit lattice, and that the arrangement is correct.The ovule grows when it becomes 11 times larger than the critical crystal. do,
Caclm; 61110 is considered to exhibit accumulated supercooling because the energy gap is large when the ovule reaches a size larger than the critical crystal diameter. The nucleating agent is thought to play a role in reducing this energy gap.

なお、核剤の添加量は一解度以上であればよく、上限に
は轡に制限はないが、実用−上10重量%以下がMまし
い、また核剤の分散tよくするため増粘剤等を添加して
もよい、増粘剤としては、蓄熱材に層解するえとえはカ
ルボキシルメチルセルロース(CMC)のような高分子
物質である。
Note that the amount of the nucleating agent to be added may be at least 1 degree of solubility, and there is no upper limit on the amount, but from a practical standpoint, it is preferably 10% by weight or less. The thickening agent may be a polymeric substance such as carboxymethyl cellulose (CMC) that is decomposed into the heat storage material.

(4)実施例 実施例1 Caclm−@HsOに対し、酢酸バリウム(Ba (
CHICoo)m)to、2重量饅加見たものt蓄熱容
器に1!閉した。COものは24Cで凝固を開始した。
(4) Examples Example 1 Barium acetate (Ba (
CHICoo) m) to, 2 weight manka saw t heat storage container 1! Closed. The CO one started coagulating at 24C.

この凝固点は11−一凝固110回くり返してもほとん
ど同じ安定な性gI!を示した0図として示したグラフ
中のB蘭−で代表される挙動がこnに該当する。なシ、
同グレアにおいてC−一は比較例と“して示し鹸もので
核剤なしの場合の挙動を示している。な2ム蘭線は融層
を表わしている・夷廁内2 実JI例1の蓄熱材組成物に、核剤の分−剤としてCM
C1G、1重′量−添加したものtS熱容器に密閉した
・このものは実施例1の蓄熱材より411E剤の分散安
定□性が゛すぐれていた。蓄熱゛轡性は実施例1の場合
と略同様で6″)た。
This solidification point remains almost the same even after repeated solidification 110 times! The behavior represented by B in the graph shown as 0 corresponds to this n. Nasi,
In the same glare, C-1 is shown as a comparative example and shows the behavior when there is no nucleating agent. CM is added to the heat storage material composition as a nucleating agent.
C1G, 1 wt.-added tS sealed in a heat container.This material had better dispersion stability of the 411E agent than the heat storage material of Example 1. The heat storage properties were approximately the same as in Example 1 (6'').

嶋)効 果 本発明はlI妃核剤を添加τているので以下の轡□做t
4する。
(Shima) Effect Since the present invention includes the addition of a lI-nucleating agent, the following effects can be achieved.
4.

H) 過冷却が防止さnる・ (−一定温度において吸熱、放熱が行われる安定した性
絽の蓄熱材となる。
H) Overcooling is prevented (- It becomes a stable heat storage material that absorbs and releases heat at a constant temperature.

(ハ)Caal16111O自体の脣性が核剤によって
影響をうけない。
(c) The flexibility of Caal16111O itself is not affected by the nucleating agent.

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

図は蓄熱材の冷却通楊における温度変化1*わ十グラフ
である。 轡許出願人       。 松下電工株式会社 代−人弁場士 竹 元 敏 丸 (ほか21名)
The figure is a graph of temperature change (1*Way) during cooling of the heat storage material. License applicant. Matsushita Electric Works Co., Ltd. Representative: Toshimaru Takemoto (and 21 other people)

Claims (1)

【特許請求の範囲】 a) 塩化カルシクム六水塩中に過冷却防止用の核剤と
しで、酢酸バリウムt−添加してなる蓄熱材。 (2)  核剤か#解度以上の量で添加されていること
tqII做とする特許請求の範囲第1項記載の蓄熱材・ (3)  増粘剤を添加したことt−4I愼とする特許
請求の軛d第1項または第2項記載の蓄熱材。
[Scope of Claims] a) A heat storage material made by adding barium acetate (T) to calcium chloride hexahydrate as a nucleating agent to prevent supercooling. (2) The heat storage material according to claim 1, in which a nucleating agent is added in an amount equal to or more than #1. The heat storage material according to claim 1 or 2 of claim d.
JP10181681A 1981-06-29 1981-06-29 Heat accumulating material Pending JPS582598A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10181681A JPS582598A (en) 1981-06-29 1981-06-29 Heat accumulating material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10181681A JPS582598A (en) 1981-06-29 1981-06-29 Heat accumulating material

Publications (1)

Publication Number Publication Date
JPS582598A true JPS582598A (en) 1983-01-08

Family

ID=14310643

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10181681A Pending JPS582598A (en) 1981-06-29 1981-06-29 Heat accumulating material

Country Status (1)

Country Link
JP (1) JPS582598A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5888929A (en) * 1996-12-18 1999-03-30 Oji Paper Co., Ltd. Sheet set for temperature control and method of using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5888929A (en) * 1996-12-18 1999-03-30 Oji Paper Co., Ltd. Sheet set for temperature control and method of using the same

Similar Documents

Publication Publication Date Title
US7923112B2 (en) Latent heat storage material and process for manufacture of the latent heat storage material
JPS582598A (en) Heat accumulating material
JPS59109578A (en) Heat storage material
JP2800039B2 (en) Latent heat storage material
JPS5842225B2 (en) heat storage device
JP2001031956A (en) Latent heat storage material composition
JPS6111276B2 (en)
JPS63137982A (en) Heat storage material composition
JPH05331457A (en) Composition for heat storage
JP2982409B2 (en) Latent heat storage material
JPH02286777A (en) Heat storage material
JPH02395B2 (en)
JPH11166176A (en) Latent-heat storage composition
JPS61197668A (en) Thermal energy storage material
JPS58225181A (en) Heat storage material
JPS60203689A (en) Thermal energy storage material
JPS5866799A (en) Heat-accumulating material
JPH04356583A (en) Latent heat storage material
JPS6351478B2 (en)
JPS59170181A (en) Heat accumulative agent composition
JPS59140283A (en) Thermal energy storage material
JPS6236486A (en) Heat storing material
JPS59212697A (en) Constituent of heat accumulating agent
JPS60163989A (en) Phase transition heat storing material
JPS5845499A (en) Heat accumulating material