JP3473283B2 - Heat storage material composition - Google Patents
Heat storage material compositionInfo
- Publication number
- JP3473283B2 JP3473283B2 JP19358996A JP19358996A JP3473283B2 JP 3473283 B2 JP3473283 B2 JP 3473283B2 JP 19358996 A JP19358996 A JP 19358996A JP 19358996 A JP19358996 A JP 19358996A JP 3473283 B2 JP3473283 B2 JP 3473283B2
- Authority
- JP
- Japan
- Prior art keywords
- heat storage
- storage material
- material composition
- erythritol
- melting point
- 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.)
- Expired - Lifetime
Links
- 238000005338 heat storage Methods 0.000 title claims description 36
- 239000011232 storage material Substances 0.000 title claims description 25
- 239000000203 mixture Substances 0.000 title claims description 16
- 238000002844 melting Methods 0.000 claims description 30
- 230000008018 melting Effects 0.000 claims description 30
- 239000004386 Erythritol Substances 0.000 claims description 23
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 claims description 23
- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 claims description 23
- 235000019414 erythritol Nutrition 0.000 claims description 23
- 229940009714 erythritol Drugs 0.000 claims description 23
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 18
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 14
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 12
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000011780 sodium chloride Substances 0.000 claims description 7
- 239000001103 potassium chloride Substances 0.000 claims description 6
- 235000011164 potassium chloride Nutrition 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 description 9
- 239000012071 phase Substances 0.000 description 9
- 239000002775 capsule Substances 0.000 description 8
- 230000004927 fusion Effects 0.000 description 4
- 239000003094 microcapsule Substances 0.000 description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 235000017281 sodium acetate Nutrition 0.000 description 3
- 150000005846 sugar alcohols Chemical class 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical class [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000001632 sodium acetate Substances 0.000 description 2
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
- BDKLKNJTMLIAFE-UHFFFAOYSA-N 2-(3-fluorophenyl)-1,3-oxazole-4-carbaldehyde Chemical compound FC1=CC=CC(C=2OC=C(C=O)N=2)=C1 BDKLKNJTMLIAFE-UHFFFAOYSA-N 0.000 description 1
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical class OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910021612 Silver iodide Chemical class 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical class O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 229940009859 aluminum phosphate Drugs 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- AGXUVMPSUKZYDT-UHFFFAOYSA-L barium(2+);octadecanoate Chemical compound [Ba+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AGXUVMPSUKZYDT-UHFFFAOYSA-L 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- QHFQAJHNDKBRBO-UHFFFAOYSA-L calcium chloride hexahydrate Chemical compound O.O.O.O.O.O.[Cl-].[Cl-].[Ca+2] QHFQAJHNDKBRBO-UHFFFAOYSA-L 0.000 description 1
- JUNWLZAGQLJVLR-UHFFFAOYSA-J calcium diphosphate Chemical class [Ca+2].[Ca+2].[O-]P([O-])(=O)OP([O-])([O-])=O JUNWLZAGQLJVLR-UHFFFAOYSA-J 0.000 description 1
- 239000001506 calcium phosphate Substances 0.000 description 1
- 229910000389 calcium phosphate Inorganic materials 0.000 description 1
- 235000011010 calcium phosphates Nutrition 0.000 description 1
- 229940043256 calcium pyrophosphate Drugs 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 229940095672 calcium sulfate Drugs 0.000 description 1
- HRBZRZSCMANEHQ-UHFFFAOYSA-L calcium;hexadecanoate Chemical compound [Ca+2].CCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCC([O-])=O HRBZRZSCMANEHQ-UHFFFAOYSA-L 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920003020 cross-linked polyethylene Polymers 0.000 description 1
- 239000004703 cross-linked polyethylene Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 235000019821 dicalcium diphosphate Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- FBPFZTCFMRRESA-GUCUJZIJSA-N galactitol Chemical compound OC[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-GUCUJZIJSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- -1 polyethylene Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000010408 potassium alginate Nutrition 0.000 description 1
- 239000000737 potassium alginate Substances 0.000 description 1
- MZYRDLHIWXQJCQ-YZOKENDUSA-L potassium alginate Chemical compound [K+].[K+].O1[C@@H](C([O-])=O)[C@@H](OC)[C@H](O)[C@H](O)[C@@H]1O[C@@H]1[C@@H](C([O-])=O)O[C@@H](O)[C@@H](O)[C@H]1O MZYRDLHIWXQJCQ-YZOKENDUSA-L 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical class [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- FJOLTQXXWSRAIX-UHFFFAOYSA-K silver phosphate Chemical class [Ag+].[Ag+].[Ag+].[O-]P([O-])([O-])=O FJOLTQXXWSRAIX-UHFFFAOYSA-K 0.000 description 1
- 229940019931 silver phosphate Drugs 0.000 description 1
- 229910000161 silver phosphate Inorganic materials 0.000 description 1
- YPNVIBVEFVRZPJ-UHFFFAOYSA-L silver sulfate Chemical class [Ag+].[Ag+].[O-]S([O-])(=O)=O YPNVIBVEFVRZPJ-UHFFFAOYSA-L 0.000 description 1
- 229910000367 silver sulfate Inorganic materials 0.000 description 1
- 229940087562 sodium acetate trihydrate Drugs 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 235000010288 sodium nitrite Nutrition 0.000 description 1
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000004781 supercooling Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000002918 waste heat Substances 0.000 description 1
Landscapes
- Compositions Of Macromolecular Compounds (AREA)
Description
【0001】[0001]
【発明の属する技術分野】本発明は、エリスリトールを
主成分とし、その融解潜熱を利用する蓄熱材組成物に関
する。TECHNICAL FIELD The present invention relates to a heat storage material composition containing erythritol as a main component and utilizing its latent heat of fusion.
【0002】[0002]
【従来の技術】潜熱蓄熱材は、顕熱型蓄熱材に比べて蓄
熱密度が高く、相変化温度が一定であるため、熱の取り
出し温度が安定であるという利点を活かして実用化され
ている。潜熱蓄熱材として、氷、硫酸ナトリウム10水
塩、塩化カルシウム6水塩及び酢酸ナトリウム3水塩な
どが知られている。しかしながら、これらの潜熱蓄熱材
の相変化温度は比較的低温であり、90〜190℃程度
と高い相変化温度が望まれる、給湯やボイラーの廃熱利
用及び太陽エネルギーを利用するための蓄熱材として
は、不適当である。2. Description of the Related Art Latent heat storage materials have been put into practical use by taking advantage of the fact that the heat extraction temperature is stable because they have a higher heat storage density and a constant phase change temperature than sensible heat storage materials. . Known latent heat storage materials include ice, sodium sulfate decahydrate, calcium chloride hexahydrate, sodium acetate trihydrate, and the like. However, the phase change temperature of these latent heat storage materials is relatively low, and a high phase change temperature of about 90 to 190 ° C. is desired, as a heat storage material for utilizing waste heat of hot water or boiler and utilizing solar energy. Is inappropriate.
【0003】そこで、高い相変化温度を有する蓄熱材組
成物として、エリスリトール、マンニトール、ガラクチ
トールなどの糖アルコールを用いることが提案されてい
る(特開平5−32963号公報、特表昭63−500
946号公報)。また、エリスリトールに固相転移点を
有するペンタエリスリトール、ペンタグリセリンおよび
ネオペンチルグリコールを配合し、これらの2成分系の
相変化温度が変化することが報告されている。(第16
回日本熱物性シンポジウム、1995年、P221)Therefore, it has been proposed to use sugar alcohols such as erythritol, mannitol and galactitol as a heat storage material composition having a high phase change temperature (Japanese Patent Laid-Open No. 5-32963, Japanese Patent Publication No. 63-500).
946 publication). It has also been reported that erythritol is blended with pentaerythritol, pentaglycerin and neopentyl glycol having a solid phase transition point to change the phase change temperature of these two-component systems. (16th
Japan Thermophysical Properties Symposium, 1995, P221)
【0004】[0004]
【発明が解決しようとする課題】エリスリトールは蓄熱
量が大きく、熱安定性も優れ、無毒性であるが、相変化
温度は物質由来で一定である。そこで、糖アルコールを
蓄熱材として使用するために、相変化温度を蓄熱システ
ムに適するように調節することが求められる。第16回
日本熱物性シンポジウム(1995年、P221)で
は、エリスリトールにペンタエリスリトール、ペンタグ
リセリンおよびネオペンチルグリコールを添加すること
で、エリスリトールの相変化温度が100℃付近ほどに
低下することが報告されているが、2相共存のダブルピ
ークが見られ、蓄熱量も半分以下まで低下しているなど
解決すべき問題点が多い。Erythritol has a large heat storage amount, excellent thermal stability, and is nontoxic, but the phase change temperature is constant due to the substance. Therefore, in order to use sugar alcohol as a heat storage material, it is required to adjust the phase change temperature so as to be suitable for the heat storage system. At the 16th Symposium on Thermophysical Properties (1995, P221), it was reported that the addition of pentaerythritol, pentaglycerin and neopentyl glycol to erythritol lowered the phase change temperature of erythritol to around 100 ° C. However, there are many problems to be solved, such as the double peak of coexistence of two phases and the reduction of the amount of heat storage to less than half.
【0005】[0005]
【課題を解決するための手段】本発明者らは、上記課題
に鑑み鋭意検討した結果、エリスリトールに融点調整剤
としてエチレングリコール、塩化ナトリウムおよび塩化
カリウムから選ばれる一種以上を添加すると、エリスリ
トールの融点が95〜110℃まで低下することを見出
し本発明に到達した。Means for Solving the Problems As a result of intensive studies in view of the above problems, the present inventors have found that when erythritol is added with one or more selected from ethylene glycol, sodium chloride and potassium chloride as a melting point adjusting agent, the melting point of erythritol is increased. The present invention has been achieved by finding that the temperature decreases to 95 to 110 ° C.
【0006】すなわち、本発明の要旨は、融点調整剤と
してエリスリトールにエチレングリコール、塩化ナトリ
ウムおよび塩化カリウムから選ばれる1種以上を含有し
てなる蓄熱材組成物に存する。That is, the gist of the present invention resides in a heat storage material composition comprising erythritol as a melting point adjusting agent and at least one selected from ethylene glycol, sodium chloride and potassium chloride.
【0007】[0007]
【発明の実施の態様】本発明においては、主成分のエリ
スリトールに融点調整剤としてエチレングリコール、塩
化ナトリウムおよび塩化カリウムから選ばれる1種以上
を添加することを特徴とする。融点調整剤の含有量は、
通常1〜30重量%、好ましくは3〜20重量%であ
る。融点調整剤の含有量が30重量%より多いと、蓄熱
材組成物中の糖アルコールの含有量が減少して蓄熱量が
小さくなり、一方、1重量%より少ないと、融点を降下
させる効果が得られない。BEST MODE FOR CARRYING OUT THE INVENTION In the present invention, one or more selected from ethylene glycol, sodium chloride and potassium chloride as a melting point adjusting agent is added to erythritol as a main component. The content of the melting point adjusting agent is
It is usually 1 to 30% by weight, preferably 3 to 20% by weight. When the content of the melting point adjusting agent is more than 30% by weight, the content of sugar alcohol in the heat storage material composition is reduced and the heat storage amount is small, while when it is less than 1% by weight, the effect of lowering the melting point is obtained. I can't get it.
【0008】本発明の蓄熱材組成物は、パラフィン、ポ
リエチレングリコール、ポリビニルアルコール、ポリエ
チレン、架橋ポリエチレンなどの公知の蓄熱材と併用し
てもよい。また、炭酸カルシウム、リン酸カルシウム、
硫酸カルシウム、ピロリン酸カルシウム、リン酸アルミ
ニウム、リン酸銀、硫酸銀、塩化銀またはヨウ化銀など
の無機塩やステアリン酸カルシウム、ステアリン酸マグ
ネシウム、ステアリン酸バリウムまたはパルミチン酸カ
ルシウムなどの長鎖脂肪酸の有機塩などの過冷却防止
剤、水不溶性吸水性樹脂、カルボキシメチルセルロー
ス、アルギン酸ナトリウム、アルギン酸カリウム、微粉
シリカなどの増粘剤、フェノール類、アミン類、ヒドロ
キシアミン類などの酸化防止剤、クロム酸塩、ポリリン
酸塩、亜硝酸ナトリウムなどの金属腐食防止剤などの添
加剤を含有してもよい。The heat storage material composition of the present invention may be used in combination with a known heat storage material such as paraffin, polyethylene glycol, polyvinyl alcohol, polyethylene and crosslinked polyethylene. Also, calcium carbonate, calcium phosphate,
Inorganic salts of calcium sulfate, calcium pyrophosphate, aluminum phosphate, silver phosphate, silver sulfate, silver chloride or silver iodide and organic salts of long-chain fatty acids such as calcium stearate, magnesium stearate, barium stearate or calcium palmitate. Supercooling inhibitors such as water-insoluble water-absorbent resins, carboxymethyl cellulose, sodium alginate, potassium alginate, thickeners such as finely divided silica, antioxidants such as phenols, amines, hydroxyamines, chromates, polyphosphorus Additives such as acid corrosion inhibitors and metal corrosion inhibitors such as sodium nitrite may be contained.
【0009】本発明の蓄熱材組成物は、融解温度が通常
95〜110℃であり、融解潜熱量が通常45cal/
g以上である。本発明の蓄熱材組成物の調合方法は、特
に限定されないが、エリスリトール、融点調整剤、必要
に応じて添加剤や公知の蓄熱材を混合して均一に分散さ
せればよい。より均一に分散させるためには、エリスリ
トールをその融点以上の温度まで加熱し、撹拌しながら
融点調整剤や添加剤を添加混合する方法が挙げられる。The heat storage material composition of the present invention has a melting temperature of usually 95 to 110 ° C. and a latent heat of fusion of usually 45 cal /.
g or more. The method for preparing the heat storage material composition of the present invention is not particularly limited, but erythritol, a melting point adjusting agent, and if necessary, an additive and a known heat storage material may be mixed and uniformly dispersed. In order to disperse more uniformly, a method of heating erythritol to a temperature equal to or higher than its melting point and adding and mixing a melting point adjusting agent and an additive while stirring is mentioned.
【0010】本発明の蓄熱材組成物の使用方法として
は、例えば、蓄熱容器に蓄熱材組成物を充填するカプセ
ル型、蓄熱容器を必要としないマイクロカプセル型が挙
げられる。カプセル型は、蓄熱材組成物をカプセルなど
の蓄熱容器に注入し、蓄熱容器を密封することにより得
られる。カプセルの材質は、使用温度範囲で変形、溶融
しない材質であればよく、例えば、ステンレス、アルミ
ニウムなどの金属、ガラス、ポリカーボネートなどのエ
ンジニアリングプラスチックなどが挙げられる。カプセ
ルの形状は、特に限定されず、例えば、球状、板状、パ
イプ状、くびれ筒状、双子球状、波板状などが挙げら
れ、用途に応じて適宜選択される。マイクロカプセル型
は、微細な蓄熱材の粒子またはその集合体を、使用温度
範囲で溶融、劣化しない樹脂などの被膜で覆ったもの
で、カプセル型に比べ表面積が極めて大きくなるので、
熱伝達効率が高いという利点がある。Examples of the method of using the heat storage material composition of the present invention include a capsule type in which a heat storage container is filled with the heat storage material composition and a microcapsule type in which the heat storage container is not required. The capsule type is obtained by injecting the heat storage material composition into a heat storage container such as a capsule and sealing the heat storage container. The material of the capsule may be any material that does not deform or melt within the operating temperature range, and examples thereof include metals such as stainless steel and aluminum, glass, and engineering plastics such as polycarbonate. The shape of the capsule is not particularly limited, and examples thereof include a spherical shape, a plate shape, a pipe shape, a constricted cylinder shape, a twin spherical shape, and a corrugated plate shape, and are appropriately selected depending on the application. The microcapsule type is a particle of fine heat storage material or an aggregate thereof, which is covered with a film such as a resin that does not melt or deteriorate in the operating temperature range, and has a very large surface area compared to the capsule type.
It has the advantage of high heat transfer efficiency.
【0011】蓄熱システムにおいては、カプセルやマイ
クロカプセルのまわりを熱媒体が流れ、カプセルやマイ
クロカプセルを被覆する樹脂が熱交換器の役目を果た
し、蓄熱、放熱が行われる。熱媒体としては、水、水蒸
気、空気などのガスが挙げられる。In the heat storage system, the heat medium flows around the capsules and the microcapsules, and the resin coating the capsules and the microcapsules serves as a heat exchanger to store and radiate heat. Examples of the heat medium include gases such as water, steam and air.
【0012】[0012]
【実施例】以下、実施例により本発明をさらに詳細に説
明するが、本発明はその要旨を超えない限り、以下の実
施例に限定されるものではない。エリスリトールは日研
化学株式会社製、エチレングリコール、塩化カリウム、
ポリエチレングリコールは和光純薬工業株式会社製試
薬、塩化ナトリウムはマナック株式会社製試薬、臭化ナ
トリウム、酢酸ナトリウムはキシダ化学株式会社製試薬
を用いた。The present invention will be described in more detail with reference to the following examples, but the present invention is not limited to the following examples unless it exceeds the gist thereof. Erythritol is manufactured by Nikken Chemical Co., Ltd., ethylene glycol, potassium chloride,
Polyethylene glycol used was a reagent manufactured by Wako Pure Chemical Industries, Ltd., sodium chloride used was a reagent manufactured by Manac Co., Ltd., sodium bromide, and sodium acetate were reagents manufactured by Kishida Chemical Co., Ltd.
【0013】実施例1
エリスリトール4.875gと塩化ナトリウム0.12
5g(エリスリトールに対して2.5重量%)を室温に
おいて乳鉢で均質になるまで混合した。得られた蓄熱材
組成物の融解温度と融解潜熱量をアルミニウムの密封セ
ルを使用し、示差走査熱量計(セイコー電子工業社製、
DSC−220C)で測定した。結果を表−1に示す。
実施例2〜6
エリスリトールと塩化ナトリウムを表−1に示す割合と
した他は実施例1と同様に行った。融解温度と融解潜熱
量を表−1に示す。
実施例7〜9
エリスリトールとエチレングリコールを表−1に示す割
合とした他は実施例1と同様に行った。融解温度と融解
潜熱量を表−1に示す。Example 1 4.875 g of erythritol and 0.12 of sodium chloride
5 g (2.5% by weight with respect to erythritol) were mixed in a mortar at room temperature until homogeneous. Using a sealed cell of aluminum for the melting temperature and the latent heat of fusion of the obtained heat storage material composition, a differential scanning calorimeter (manufactured by Seiko Electronics Co., Ltd.,
It was measured by DSC-220C). The results are shown in Table-1. Examples 2 to 6 The same procedure as in Example 1 was carried out except that the ratios of erythritol and sodium chloride shown in Table 1 were used. The melting temperature and the latent heat of melting are shown in Table-1. Examples 7 to 9 The same procedure as in Example 1 was carried out except that the ratios of erythritol and ethylene glycol shown in Table 1 were used. The melting temperature and the latent heat of melting are shown in Table-1.
【0014】実施例10〜12
エリスリトールと塩化カリウムを表−1に示す割合とし
た他は実施例1と同様に行った。融解温度と融解潜熱量
を表−1に示す。
比較例1〜3
エリスリトールとポリエチレングリコールを表−1に示
す割合とした他は実施例1と同様に行った。融解温度と
融解潜熱量を表−1に示す。
比較例4、5
エリスリトールと臭化ナトリウムを表−1に示す割合と
した他は実施例1と同様に行った。融解温度と融解潜熱
量を表−1に示す。
比較例6、7
エリスリトールと酢酸ナトリウムを表−1に示す割合と
した他は実施例1と同様に行った。融解温度と融解潜熱
量を表−1に示す。Examples 10 to 12 The same procedure as in Example 1 was carried out except that the ratios of erythritol and potassium chloride shown in Table 1 were used. The melting temperature and the latent heat of melting are shown in Table-1. Comparative Examples 1 to 3 The procedure of Example 1 was repeated except that the ratios of erythritol and polyethylene glycol shown in Table 1 were used. The melting temperature and the latent heat of melting are shown in Table-1. Comparative Examples 4 and 5 The same procedure as in Example 1 was carried out except that the ratios of erythritol and sodium bromide shown in Table 1 were used. The melting temperature and the latent heat of melting are shown in Table-1. Comparative Examples 6 and 7 The procedure of Example 1 was repeated, except that the ratios of erythritol and sodium acetate shown in Table 1 were used. The melting temperature and the latent heat of melting are shown in Table-1.
【0015】[0015]
【表1】
*:融点が2カ所に現れたため、それぞれの融点におけ
る融解潜熱量が測定できなかったことを示す。[Table 1] *: The melting points appeared at two places, so the latent heat of fusion at each melting point could not be measured.
【0016】[0016]
【発明の効果】本発明によれば、相分離することなく、
また、蓄熱量を低下させずに、エリスリトールを主成分
とする蓄熱材組成物の融点を調整することができる。According to the present invention, without phase separation,
Further, the melting point of the heat storage material composition containing erythritol as a main component can be adjusted without lowering the heat storage amount.
フロントページの続き (56)参考文献 特開 平5−32963(JP,A) 特開 昭63−218786(JP,A) 特開 昭61−238882(JP,A) 特開 平1−223190(JP,A) 実開 平5−5115(JP,U) (58)調査した分野(Int.Cl.7,DB名) C09K 5/06 Continuation of the front page (56) Reference JP-A-5-32963 (JP, A) JP-A-63-218786 (JP, A) JP-A-61-238882 (JP, A) JP-A-1-223190 (JP , A) Actual Kaihei 5-5115 (JP, U) (58) Fields investigated (Int.Cl. 7 , DB name) C09K 5/06
Claims (3)
塩化ナトリウムおよび塩化カリウムから選ばれる少なく
とも一種以上を含有することを特徴とするエリスリトー
ルを主成分とする蓄熱材組成物。1. Ethylene glycol as a melting point adjusting agent,
A heat storage material composition containing erythritol as a main component, which comprises at least one selected from sodium chloride and potassium chloride.
ある請求項1に記載の蓄熱材組成物。2. The heat storage material composition according to claim 1, wherein the blending amount of the melting point adjusting agent is 1 to 30% by weight.
たは2に記載の蓄熱材組成物。3. The heat storage material composition according to claim 1, which has a melting point of 95 to 110 ° C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19358996A JP3473283B2 (en) | 1996-07-23 | 1996-07-23 | Heat storage material composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP19358996A JP3473283B2 (en) | 1996-07-23 | 1996-07-23 | Heat storage material composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH1036824A JPH1036824A (en) | 1998-02-10 |
| JP3473283B2 true JP3473283B2 (en) | 2003-12-02 |
Family
ID=16310490
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP19358996A Expired - Lifetime JP3473283B2 (en) | 1996-07-23 | 1996-07-23 | Heat storage material composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP3473283B2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001081446A (en) * | 1999-09-16 | 2001-03-27 | Matsushita Electric Ind Co Ltd | Heat storage material composition and heat storage body |
| JP5134808B2 (en) * | 2006-10-16 | 2013-01-30 | 玉井化成株式会社 | Thermal storage material composition containing sugar alcohol |
| JP5556613B2 (en) * | 2010-11-18 | 2014-07-23 | 株式会社デンソー | Semiconductor device |
| IT201800009211A1 (en) * | 2018-10-05 | 2020-04-05 | Groppalli Srl | INERT BLEND AND ITS USE AS A PHASE CHANGE MATERIAL |
| IT202000006259A1 (en) * | 2020-03-25 | 2021-09-25 | Groppalli S R L | INERT MIX AND ITS USE AS A PHASE CHANGE MATERIAL FOR HIGH TEMPERATURE APPLICATIONS |
-
1996
- 1996-07-23 JP JP19358996A patent/JP3473283B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH1036824A (en) | 1998-02-10 |
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