JP2779990B2 - Heat storage component and heat storage material - Google Patents
Heat storage component and heat storage materialInfo
- Publication number
- JP2779990B2 JP2779990B2 JP4200348A JP20034892A JP2779990B2 JP 2779990 B2 JP2779990 B2 JP 2779990B2 JP 4200348 A JP4200348 A JP 4200348A JP 20034892 A JP20034892 A JP 20034892A JP 2779990 B2 JP2779990 B2 JP 2779990B2
- Authority
- JP
- Japan
- Prior art keywords
- heat storage
- parts
- storage component
- storage material
- heat
- 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 76
- 239000011232 storage material Substances 0.000 title claims description 30
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 14
- 150000002430 hydrocarbons Chemical class 0.000 claims description 14
- 239000012188 paraffin wax Substances 0.000 claims description 13
- 239000008247 solid mixture Substances 0.000 claims description 12
- 229920000620 organic polymer Polymers 0.000 claims description 9
- 238000000034 method Methods 0.000 description 25
- CBFCDTFDPHXCNY-UHFFFAOYSA-N icosane Chemical compound CCCCCCCCCCCCCCCCCCCC CBFCDTFDPHXCNY-UHFFFAOYSA-N 0.000 description 14
- 238000010438 heat treatment Methods 0.000 description 13
- 238000002156 mixing Methods 0.000 description 10
- 229920001971 elastomer Polymers 0.000 description 7
- 239000005060 rubber Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- -1 silica Chemical class 0.000 description 6
- 229920002725 thermoplastic elastomer Polymers 0.000 description 5
- 150000001336 alkenes Chemical class 0.000 description 4
- 238000004898 kneading Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 239000011805 ball Substances 0.000 description 3
- 229960000541 cetyl alcohol Drugs 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- RZJRJXONCZWCBN-UHFFFAOYSA-N octadecane Chemical compound CCCCCCCCCCCCCCCCCC RZJRJXONCZWCBN-UHFFFAOYSA-N 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- IRFSXVIRXMYULF-UHFFFAOYSA-N 1,2-dihydroquinoline Chemical compound C1=CC=C2C=CCNC2=C1 IRFSXVIRXMYULF-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 241000283984 Rodentia Species 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229920003244 diene elastomer Polymers 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical compound C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 239000012784 inorganic fiber Substances 0.000 description 1
- 229920003049 isoprene rubber Polymers 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003094 microcapsule Substances 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229940038384 octadecane Drugs 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000000191 radiation effect Effects 0.000 description 1
- 230000003014 reinforcing effect Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 229940012831 stearyl alcohol Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Central Heating Systems (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は、暖房用等に好適な蓄熱
成分、及びそれを固体状態で保持して取扱性に優れる蓄
熱材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat storage component suitable for heating and the like, and a heat storage material which retains it in a solid state and has excellent handleability.
【0002】[0002]
【従来の技術】従来、温水パイプや電気ヒーター等を敷
設した上に床板等を設けてなる床暖房システムが提案さ
れていた。しかしながら、ガスや石油やヒートポンプ等
による温水の形成、あるいは電気ヒーターによる加温に
多量のエネルギーを要し、エネルギーの消費量が大きい
問題点があった。かかるエネルギーの大量消費は、ラン
ニングコストの増大などとして表出する。2. Description of the Related Art There has been proposed a floor heating system in which a floor plate and the like are provided on a hot water pipe, an electric heater, and the like. However, there is a problem that a large amount of energy is required for forming hot water using gas, oil, a heat pump, or the like, or for heating using an electric heater, resulting in large energy consumption. Such a large consumption of energy is manifested as an increase in running cost.
【0003】[0003]
【発明が解決しようとする課題】前記に鑑みて本発明者
らは、エネルギー消費量の節約をはかるべく鋭意検討を
重ねて蓄熱成分の凝固熱を利用する方式に想到した。す
なわち、液体状態の蓄熱成分が高温を維持しつつ潜熱を
放出して凝固することに着目し、その凝固熱(潜熱)に
基づいて蓄熱する方式に想到した。かかる方式によれ
ば、夜間の余剰電力等を利用して蓄熱成分を溶解させ、
それが冷却固化(凝固)する際の放熱作用による暖房シ
ステムの構築なども可能になる。In view of the above, the present inventors have made intensive studies to save energy consumption and have conceived of a system utilizing the heat of solidification of a heat storage component. That is, the inventors focused on the fact that the heat storage component in the liquid state releases latent heat and solidifies while maintaining a high temperature, and conceived a method of storing heat based on the heat of solidification (latent heat). According to such a method, the heat storage component is dissolved using surplus power at night,
It becomes possible to construct a heating system by the heat radiation effect when it is cooled and solidified (solidified).
【0004】しかし蓄熱成分は、融解して液体状態とな
るためそのままでは実用に供しにくく、前記方式の実用
化には蓄熱成分が融解して液体状態となっても流出を防
止できる蓄熱材であることが必要である。また本発明者
らは鋭意研究の結果、暖房等による室温は19〜23℃
が適当で、かかる室温を建物の構造等を考慮して実現す
るためには蓄熱材の蓄熱温度を35〜45℃に設定する
ことが好ましいことを究明した。しかし公知の蓄熱成分
を用いて前記の目的を達成することはできないことが判
明した(特公昭55−116786号公報、特公昭56
−16089号公報)。However, the heat storage component is difficult to be put to practical use as it is because it is melted to be in a liquid state. For practical use of the above method, even if the heat storage component is melted to be in a liquid state, it is a heat storage material capable of preventing outflow. It is necessary. In addition, as a result of intensive studies, the present inventors found that the room temperature due to heating or the like was 19 to 23 ° C.
It has been found that it is preferable to set the heat storage temperature of the heat storage material to 35 to 45 ° C. in order to realize such room temperature in consideration of the structure of the building and the like. However, it has been found that the above object cannot be achieved using a known heat storage component (Japanese Patent Publication No. Sho 55-116786, Japanese Patent Publication No. Sho 56-116).
-16089).
【0005】従って本発明は、蓄熱成分が融解して液体
状態となっても流出せず、蓄熱温度が35〜45℃で蓄
熱量に優れる、蓄熱方式の暖房システムなどに好ましく
用いうる蓄熱成分、ないし蓄熱材の開発を課題とする。Accordingly, the present invention provides a heat storage component which is preferably used for a heat storage type heating system and the like, which does not flow out even if the heat storage component is melted to be in a liquid state, has a heat storage temperature of 35 to 45 ° C. and is excellent in heat storage. Or the development of heat storage materials.
【0006】[0006]
【課題を解決するための手段】本発明は、115°Fパ
ラフィンワックス100重量部あたり、エイコサンを2
0〜150重量部含有することを特徴とする蓄熱成分、
及びかかる蓄熱成分と炭化水素系有機高分子との固体状
混合物からなることを特徴とする蓄熱材を提供するもの
である。SUMMARY OF THE INVENTION The present invention relates to a method for producing eicosane at a rate of 2 parts per 100 parts by weight of 115 ° F paraffin wax.
Heat storage component characterized by containing 0 to 150 parts by weight,
And a heat storage material comprising a solid mixture of such a heat storage component and a hydrocarbon-based organic polymer.
【0007】[0007]
【作用】蓄熱成分を炭化水素系有機高分子と混合して固
体状混合物とすることにより、蓄熱成分が融解して液体
状態となっても全体としては固体状体を保持し、取扱い
性に優れて種々の形態に容易に成形できる蓄熱材を得る
ことができる。そしてその場合に、蓄熱成分として入手
が容易な115°Fパラフィンワックス100重量部に
エイコサンを20〜150重量部配合したものを用いる
ことにより、蓄熱温度が35〜45℃で蓄熱量に優れる
蓄熱材を形成することができる。[Function] By mixing a heat storage component with a hydrocarbon-based organic polymer to form a solid mixture, even if the heat storage component is melted to be in a liquid state, the solid state material is retained as a whole, and the handleability is excellent. Thus, a heat storage material that can be easily formed into various forms can be obtained. In this case, a heat storage material having a heat storage temperature of 35 to 45 ° C. and an excellent heat storage amount is used by blending 20 to 150 parts by weight of eicosan in 100 parts by weight of 115 ° F. paraffin wax, which is easily available as a heat storage component. Can be formed.
【0008】[0008]
【発明の構成要素の例示】本発明の蓄熱材は、115°
Fパラフィンワックス100重量部あたり、エイコサン
を20〜150重量部含有する蓄熱成分を炭化水素系有
機高分子と混合した固体状のものからなる。The heat storage material of the present invention has a temperature of 115 °.
It is made of a solid material in which a heat storage component containing 20 to 150 parts by weight of eicosan per 100 parts by weight of F paraffin wax is mixed with a hydrocarbon organic polymer.
【0009】本発明において用いる115°Fパラフィ
ンワックス及びエイコサンは、不純物を含有していても
よい。一般には、蓄熱量の点より50%以上の純度、好
ましくは約90%以上の純度を有するものが用いられ
る。従って、通例の工業用市販品をそのまま用いること
ができる。[0009] The 115 ° F paraffin wax and eicosane used in the present invention may contain impurities. Generally, those having a purity of 50% or more, preferably about 90% or more in terms of heat storage amount are used. Therefore, conventional commercial products can be used as they are.
【0010】蓄熱成分は、115°Fパラフィンワック
ス100重量部あたり、エイコサンを20〜150重量
部、好ましくは25〜100重量部配合したものであ
る。エイコサンの配合量が前記範囲外では、暖房用途に
好適な蓄熱温度ないし蓄熱量を有する蓄熱材を形成する
ことができない。The heat storage component contains 20 to 150 parts by weight, preferably 25 to 100 parts by weight of eicosan per 100 parts by weight of 115 ° F paraffin wax. If the amount of eicosane is out of the above range, a heat storage material having a heat storage temperature or a heat storage amount suitable for heating cannot be formed.
【0011】蓄熱成分は、必要に応じて例えばカプリル
アルコール、ラウリルアルコール、ミリスチルアルコー
ル、パルミチルアルコール、セチルアルコール、ステア
リルアルコールなどの高級アルコール類を含有していて
もよい。高級アルコール類は、蓄熱温度や蓄熱量等の調
節剤として機能し、その配合量は115°Fパラフィン
ワックスの等量以下が一般的であるがこれに限定されな
い。なお蓄熱成分には、エチレン系重合体、フェノー
ル、アミン等の各種の酸化防止剤、シリカ等の増粘剤、
シラン等のカップリング剤などの適宜な添加剤を配合す
ることができる。The heat storage component may contain higher alcohols such as caprylic alcohol, lauryl alcohol, myristyl alcohol, palmityl alcohol, cetyl alcohol and stearyl alcohol, if necessary. Higher alcohols function as regulators of heat storage temperature, heat storage amount, and the like, and the blending amount is generally equal to or less than 115 ° F. paraffin wax, but is not limited thereto. The heat storage component, ethylene-based polymer, phenol, various antioxidants such as amines, thickeners such as silica,
An appropriate additive such as a coupling agent such as silane can be blended.
【0012】前記の蓄熱成分は、袋やパイプ、中空ボー
ル等の被覆体による封入形態、ポリエチレン、ポリプロ
ピレン、ポリエステル等の有機高分子からなる袋にパッ
ク詰めして冷却過程でシートや板等に成形した形態、
布、壁、板等の多孔質体に含浸させた形態、マイクロカ
プセル中に封入した形態、有機高分子と混合した形態な
ど適宜な形態で用いることができる。その場合、必要に
応じて金属等の伝熱性物質からなる均熱化層を付加する
ことができる。The above-mentioned heat storage component is enclosed in a cover such as a bag, a pipe, or a hollow ball, packed in a bag made of an organic polymer such as polyethylene, polypropylene, or polyester, and formed into a sheet or plate in a cooling process. Form,
It can be used in an appropriate form such as a form impregnated in a porous body such as a cloth, a wall, and a plate, a form encapsulated in microcapsules, and a form mixed with an organic polymer. In this case, a soaking layer made of a heat conductive material such as a metal can be added as needed.
【0013】本発明の蓄熱材は、蓄熱成分を炭化水素系
有機高分子と混合して固体状混合物としたものである。
その場合、撹拌処理、混合処理、混練処理等の機械的手
段による混合方式が好ましい。機械的手段による混合方
式によれば、大量の蓄熱成分を混合しても、成形加工性
に優れ、蓄熱成分が移行(ブリード)しにくくてベトつ
きにくい混合物を容易に得ることができる。The heat storage material of the present invention is obtained by mixing a heat storage component with a hydrocarbon organic polymer to form a solid mixture.
In this case, a mixing method using mechanical means such as a stirring process, a mixing process, and a kneading process is preferable. According to the mixing method using mechanical means, even when a large amount of heat storage component is mixed, a mixture excellent in moldability and hard to transfer (bleed) the heat storage component and hardly sticky can be easily obtained.
【0014】機械的手段による混合は例えば、溶融物と
した一方にそれに膨潤、ないし溶解する他方を撹拌混合
する方式、両者を加熱して流動状態ないし溶融物として
それらを混練、ないし撹拌混合する方式など、適宜な方
式で行ってよい。また混練には、例えば2本ロール、バ
ンバリーミキサー、押出機、2軸混練押出機などの通例
の混合機を用いることができる。Mixing by mechanical means includes, for example, a method of stirring and mixing the other, which swells or dissolves in one of the melts, and a method of kneading them in a fluid state or a melt by heating both, or stirring and mixing. And so on. For kneading, for example, a conventional mixer such as a two-roll mill, a Banbury mixer, an extruder, or a twin-screw kneading extruder can be used.
【0015】炭化水素系有機高分子としては、主鎖が基
本的に炭化水素であり、主鎖中における他の成分(例え
ばO、N、Si、ハロゲン等)の含有量10重量%以
下、就中5重量%以下のものが好ましく用いうる。その
例としては、オレフィン系ポリマー、熱可塑性エラスト
マー、炭化水素系ゴムなどがあげられる。炭化水素系有
機高分子としては、1種又は2種以上を用いることがで
き、架橋物とすることもできる。また炭化水素系のワッ
クス状高分子などを併用することもできる。As the hydrocarbon organic polymer, the main chain is basically a hydrocarbon, and the content of other components (for example, O, N, Si, halogen, etc.) in the main chain is 10% by weight or less. Among them, those having 5% by weight or less can be preferably used. Examples include olefin-based polymers, thermoplastic elastomers, hydrocarbon-based rubbers, and the like. As the hydrocarbon-based organic polymer, one or more kinds can be used, and a crosslinked product can also be used. Also, a hydrocarbon-based wax-like polymer or the like can be used in combination.
【0016】前記オレフィン系ポリマーの具体例として
は、ポリメチレン、ポリエチレン、ポリプロピレン等の
α−オレフィンのホモポリマー、オレフィン同士のコポ
リマー、α−オレフィンと酢酸ビニル、アクリル酸エチ
ル、メタクリル酸エチルの如き他種モノマーとのコポリ
マー、それらの軽度にハロゲン化されたポリマーなどが
あげられる。Specific examples of the olefin-based polymer include homopolymers of α-olefins such as polymethylene, polyethylene, and polypropylene, copolymers of olefins, and α-olefins with vinyl acetate, ethyl acrylate, and ethyl methacrylate. Copolymers with monomers, their lightly halogenated polymers, and the like.
【0017】前記熱可塑性エラストマーの具体例として
は、スチレン系、オレフィン系、ウレタン系、エステル
系等の公知物のいずれもあげることができ、少なくとも
室温から併用する蓄熱成分の凝固点よりも10℃高い温
度域でゴム弾性を有するものが好ましく用いられる。Specific examples of the thermoplastic elastomer include known ones such as styrene-based, olefin-based, urethane-based and ester-based thermoplastic elastomers, and are at least 10 ° C. higher than the freezing point of the heat storage component used together from room temperature. Those having rubber elasticity in a temperature range are preferably used.
【0018】前記炭化水素系ゴムの具体例としては、天
然ゴム、スチレン・ブタジエンゴム、ブチルゴム、イソ
プレンゴム、エチレン・プロピレンゴム、エチレン・プ
ロピレン・ジエンゴム、エチレン・酢酸ビニルゴム、エ
チレン・エチルアクリレートゴムなどがあげられる。炭
化水素系ゴム1〜20重量部とオレフィン系ポリマー1
〜20重量部の併用系、特に化学架橋法、水架橋法、照
射架橋法等による架橋系は柔軟性、保形性、成形性、強
靱性などの点より好ましく用いうる。Specific examples of the hydrocarbon rubber include natural rubber, styrene / butadiene rubber, butyl rubber, isoprene rubber, ethylene / propylene rubber, ethylene / propylene / diene rubber, ethylene / vinyl acetate rubber, ethylene / ethyl acrylate rubber and the like. can give. 1 to 20 parts by weight of hydrocarbon rubber and olefin polymer 1
A combined system of up to 20 parts by weight, particularly a cross-linked system by a chemical cross-linking method, a water cross-linking method, an irradiation cross-linking method or the like can be preferably used from the viewpoint of flexibility, shape retention, moldability, toughness and the like.
【0019】固体状混合物は、ガスや発泡剤等による発
泡化、シラスバルーン等の添加などによる低比重化、あ
るいは金属やセラミック等の無機系高密度充填材等の添
加による高比重化などにより比重を調節することもでき
る。また、有機繊維や無機繊維の充填、あるいは紐、ワ
イヤ、不織布、織布、網等の支持体の使用による補強形
態とすることもできる。その他、固体状混合物には種々
の添加剤、酸化防止剤、着色剤、顔料、帯電防止剤、防
黴剤、難燃剤、防鼠剤、金属やカーボン等の伝熱材など
の適宜な配合剤を添加して実用に供することができる。The specific gravity of the solid mixture is increased by foaming with a gas or a foaming agent, by reducing the specific gravity by adding a shirasu balloon or the like, or by increasing the specific gravity by adding an inorganic high-density filler such as metal or ceramic. Can also be adjusted. Further, the reinforcing form can be made by filling with organic fibers or inorganic fibers or using a support such as a string, a wire, a nonwoven fabric, a woven fabric, or a net. In addition, appropriate additives such as various additives, antioxidants, coloring agents, pigments, antistatic agents, fungicides, flame retardants, rodents, heat transfer materials such as metals and carbon are added to the solid mixture. For practical use.
【0020】また固体状混合物は、ペレット等の粉末な
いし顆粒物やボール等の塊のほか、流し込み方式、プレ
ス方式、押出成形方式、射出成形方式等の適宜な方式
で、紐、シート、板、棒、ハニカム体、パイプ等の任意
な形態に加工して実用に供することができる。さらに溶
融物の流し込み方式等により、適用箇所に直接展開する
方式なども採ることができる。従って本発明の蓄熱材
は、使用目的に応じた任意な形態に成形することができ
る。The solid mixture may be used in the form of powder, granules or balls such as pellets, chunks such as balls, or any other suitable method such as a casting method, a pressing method, an extrusion molding method, or an injection molding method. It can be processed into an arbitrary form such as a honeycomb body, a pipe or the like and put to practical use. In addition, a method of directly spreading to an application location by a casting method of a molten material or the like can also be adopted. Therefore, the heat storage material of the present invention can be formed into an arbitrary form according to the purpose of use.
【0021】本発明の蓄熱材は、蓄熱式熱源として暖房
や保温などの種々の目的に用いることができる。床暖房
への適用方式としては例えば、温水の配管を蓄熱材で形
成する方式、温水中に顆粒物等からなる蓄熱材を投入し
て循環させる方式、シート等からなる蓄熱材で温水配管
を被覆する方式、床仕上げ材の下に温水配管やヒーター
等からなる適宜な熱源と共に板、棒、ハニカム体、パイ
プ等からなる蓄熱材を敷設する方式などがあげられる。The heat storage material of the present invention can be used as a heat storage heat source for various purposes such as heating and heat retention. Examples of a method for applying to the floor heating include a method in which a pipe of hot water is formed of a heat storage material, a method in which a heat storage material formed of granules or the like is circulated in hot water, and a method in which the hot water pipe is covered with a heat storage material formed of a sheet or the like. Examples of the method include a method in which a heat storage material such as a plate, a rod, a honeycomb body, or a pipe is laid along with an appropriate heat source such as a hot water pipe or a heater below a floor finishing material.
【0022】[0022]
【発明の効果】本発明によれば、蓄熱成分が液体状態と
なっても流出させずに保持して固体状体を維持する蓄熱
材を得ることができ、その取扱性に優れると共に、成形
性に優れて種々の形態で利用でき、蓄熱量、形状保持性
に優れている。また暖房に好適な蓄熱温度を有して、夜
間の余剰電力や余剰熱等を利用して経済的に蓄熱するこ
とができる。According to the present invention, it is possible to obtain a heat storage material that maintains a solid state by holding the heat storage component without flowing out even if the heat storage component is in a liquid state, and has excellent handleability and moldability. It can be used in various forms and is excellent in heat storage and shape retention. In addition, it has a heat storage temperature suitable for heating, and can store heat economically using surplus electric power and surplus heat at night.
【0023】[0023]
【実施例】 実施例1 115°Fパラフィンワックス80部(重量部、以下同
じ)と、純度98%のエイコサン(主な不純物:オクタ
デカン、ヘキサデカン、ガスクロマトグラフィーによる
測定、以下同じ)20部と、熱可塑性エラストマー(シ
ェル化学社製、クレイトンG1650、以下同じ)15
部と、炭化水素系ワックス(三井石油化学工業社製、ハ
イワックス400P、軟化点136℃、以下同じ)5部
を加熱溶融下に、酸化防止剤(2,2,4−トリメチル
−1,2−ジヒドロキノリンの重合物、以下同じ)0.
5部と共に撹拌混合して蓄熱材(固体状混合物)を得
た。Example 1 80 parts of 115 ° F paraffin wax (parts by weight, the same applies hereinafter) and 20 parts of 98% pure eicosane (main impurities: octadecane, hexadecane, measurement by gas chromatography, the same applies hereinafter), Thermoplastic elastomer (Clayton G1650, manufactured by Shell Chemical Co., Ltd .; the same applies hereinafter) 15
And 5 parts of a hydrocarbon wax (manufactured by Mitsui Petrochemical Co., Ltd., High Wax 400P, softening point: 136 ° C .; the same applies hereinafter) while heating and melting the mixture to obtain an antioxidant (2,2,4-trimethyl-1,2). -A polymer of dihydroquinoline, the same applies hereinafter)
The mixture was stirred and mixed with 5 parts to obtain a heat storage material (solid mixture).
【0024】実施例2 115°Fパラフィンワックスの使用量を70部とし、
純度98%のエイコサンの使用量を30部としたほかは
実施例1に準じて蓄熱材(固体状混合物)を得た。Example 2 The amount of 115 ° F paraffin wax used was 70 parts,
A heat storage material (solid mixture) was obtained in the same manner as in Example 1 except that the amount of eicosane having a purity of 98% was changed to 30 parts.
【0025】実施例3 115°Fパラフィンワックスの使用量を60部とし、
純度98%のエイコサンの使用量を40部としたほかは
実施例1に準じて蓄熱材(固体状混合物)を得た。Example 3 The amount of 115 ° F paraffin wax used was 60 parts,
A heat storage material (solid mixture) was obtained in the same manner as in Example 1 except that the amount of eicosane having a purity of 98% was changed to 40 parts.
【0026】実施例4 115°Fパラフィンワックスの使用量を50部とし、
純度98%のエイコサンの使用量を50部としたほかは
実施例1に準じて蓄熱材(固体状混合物)を得た。Example 4 The amount of 115 ° F paraffin wax used was 50 parts,
A heat storage material (solid mixture) was obtained in the same manner as in Example 1 except that the amount of eicosane having a purity of 98% was changed to 50 parts.
【0027】実施例5 115°Fパラフィンワックス60部と、純度98%の
エイコサン20部と、セチルアルコール20部と、熱可
塑性エラストマー15部と、炭化水素系ワックス5部を
加熱溶融下に、酸化防止剤0.5部と共に撹拌混合して
蓄熱材(固体状混合物)を得た。EXAMPLE 5 60 parts of 115 ° F. paraffin wax, 20 parts of eicosan having a purity of 98%, 20 parts of cetyl alcohol, 15 parts of a thermoplastic elastomer, and 5 parts of a hydrocarbon wax were oxidized while heating and melting. The mixture was stirred and mixed with 0.5 part of the inhibitor to obtain a heat storage material (solid mixture).
【0028】比較例1 115°Fパラフィンワックスをそのまま蓄熱材として
用いた。Comparative Example 1 115 ° F. paraffin wax was used as it was as a heat storage material.
【0029】比較例2 純度98%のエイコサンをそのまま蓄熱材として用い
た。Comparative Example 2 Eicosan having a purity of 98% was directly used as a heat storage material.
【0030】評価試験 実施例、比較例で得た蓄熱材について下記の特性を調べ
た。 蓄熱温度 JIS K 7121に準拠して示差走査熱量計にて0
〜60℃間を2℃/分の速度で昇温又は降温し、その際
のピーク温度の平均を求めた。Evaluation Test The following characteristics were examined for the heat storage materials obtained in Examples and Comparative Examples. Heat storage temperature 0 with a differential scanning calorimeter according to JIS K 7121
The temperature was raised or lowered between 2 and 60 ° C. at a rate of 2 ° C./min, and the average of the peak temperatures at that time was determined.
【0031】蓄熱量 JIS K 7122に準拠して前記の蓄熱温度試験に
おける全吸熱量と全放熱量を調べ、その平均を求めた。Heat storage amount The total heat absorption and total heat release in the above-mentioned heat storage temperature test were examined in accordance with JIS K 7122, and the average was determined.
【0032】形状保持性 1cm角ブロックの蓄熱材を60℃で1日間放置したの
ち、形状の変化を調べ、ほぼ原形を保持しているものを
良、流動又は形状変化したものを不良として評価した。Shape Retention After a 1 cm square block of heat storage material was allowed to stand at 60 ° C. for 1 day, the change in shape was examined, and the material that substantially retained the original shape was evaluated as good, and the one that had flow or changed shape was evaluated as poor. .
【0033】ブリード性 蓄熱材を60℃で7日間放置したのち、蓄熱成分が滲み
出るか否かを調べ、滲み出ないものを良とした。Bleedability After the heat storage material was allowed to stand at 60 ° C. for 7 days, it was checked whether or not the heat storage component had oozed out.
【0034】加工性 蓄熱材形成用の混合成分を150℃で撹拌混合したのち
常温に放置して固化させ、それを切り取って混合成分の
分散状態を調べ、均一に分散している場合を良とした。Workability The mixed components for forming the heat storage material are stirred and mixed at 150 ° C., then left to stand at room temperature to solidify, cut off and examined for the dispersed state of the mixed components. did.
【0035】前記の結果を表1に示した。The results are shown in Table 1.
【表1】 [Table 1]
Claims (2)
量部あたり、エイコサンを20〜150重量部含有する
ことを特徴とする蓄熱成分。1. A heat storage component comprising 20 to 150 parts by weight of eicosan per 100 parts by weight of 115 ° F. paraffin wax.
有機高分子との固体状混合物からなることを特徴とする
蓄熱材。2. A heat storage material comprising a solid mixture of the heat storage component according to claim 1 and a hydrocarbon organic polymer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4200348A JP2779990B2 (en) | 1992-07-02 | 1992-07-02 | Heat storage component and heat storage material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4200348A JP2779990B2 (en) | 1992-07-02 | 1992-07-02 | Heat storage component and heat storage material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0617042A JPH0617042A (en) | 1994-01-25 |
JP2779990B2 true JP2779990B2 (en) | 1998-07-23 |
Family
ID=16422805
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JP4200348A Expired - Lifetime JP2779990B2 (en) | 1992-07-02 | 1992-07-02 | Heat storage component and heat storage material |
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JP (1) | JP2779990B2 (en) |
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---|---|---|---|---|
AU2001294642A1 (en) * | 2000-09-21 | 2002-04-02 | Outlast Technologies, Inc. | Stable phase change materials for use in temperature regulating synthetic fibers, fabrics and textiles |
JP2008239860A (en) * | 2007-03-28 | 2008-10-09 | Toyokazutada Kk | Heat-storage medium |
CN104937065B (en) * | 2012-12-11 | 2018-08-31 | 株式会社钟化 | Heat-storing material composition, heat-storing material and transport box |
-
1992
- 1992-07-02 JP JP4200348A patent/JP2779990B2/en not_active Expired - Lifetime
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