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JPS6410752B2 - - Google Patents
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JPS6410752B2 - - Google Patents

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Publication number
JPS6410752B2
JPS6410752B2 JP57211560A JP21156082A JPS6410752B2 JP S6410752 B2 JPS6410752 B2 JP S6410752B2 JP 57211560 A JP57211560 A JP 57211560A JP 21156082 A JP21156082 A JP 21156082A JP S6410752 B2 JPS6410752 B2 JP S6410752B2
Authority
JP
Japan
Prior art keywords
coating layer
resin
adhesion
layer
polyethylene resin
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
Application number
JP57211560A
Other languages
Japanese (ja)
Other versions
JPS59100362A (en
Inventor
Masao Maki
Ju Fukuda
Yasunori Kaneko
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 JP57211560A priority Critical patent/JPS59100362A/en
Priority to AU18846/83A priority patent/AU1884683A/en
Priority to US06/606,773 priority patent/US4556048A/en
Priority to PCT/JP1983/000268 priority patent/WO1984000804A1/en
Publication of JPS59100362A publication Critical patent/JPS59100362A/en
Publication of JPS6410752B2 publication Critical patent/JPS6410752B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F24HEATING; RANGES; VENTILATING
    • F24SSOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
    • F24S70/00Details of absorbing elements
    • F24S70/20Details of absorbing elements characterised by absorbing coatings; characterised by surface treatment for increasing absorption
    • F24S70/225Details of absorbing elements characterised by absorbing coatings; characterised by surface treatment for increasing absorption for spectrally selective absorption
    • 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
    • Y02BCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
    • Y02B10/00Integration of renewable energy sources in buildings
    • Y02B10/20Solar thermal
    • 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

Landscapes

  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Sustainable Development (AREA)
  • Sustainable Energy (AREA)
  • Thermal Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Combustion & Propulsion (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

産業上の利用分野 本発明は、家庭用給湯装置としての太陽熱集熱
器の太陽熱集熱板に関するものである。 従来例の構成とその問題点 従来のプラスチツク製の太陽熱集熱板では、高
密度ポリエチレン樹脂にカーボンブラツク等を充
填し、ブロー成型で製造されているが、その表面
には太陽光の選択吸収能がなかつた。 また、この表面に選択吸収能を実現する手段と
して、塗装による手段があつたが、基材層の高密
度ポリエチレン樹脂の非粘着性が大きく、十分な
密着性が得られなかつた。 発明の目的 本発明は、高密度ポリエチレン樹脂との密着性
を高め、安価で、かつ太陽光の選択吸収能を有す
る被覆層を高密度ポリエチレン樹脂の基材層上に
設けた太陽熱集熱板を提供することを目的とする
ものである。 発明の構成 上記目的を達成するために本発明は、高密度ポ
リエチレン樹脂を主成分とする基材層の表面を
250μm以下の凹凸面として、この基材層上に、
太陽光の選択吸収能を有する被覆層を設けたもの
である。 実施例の説明 以下、本発明の実施例を説明する。図には、3
つの層が示されており、1は高密度ポリエチレン
樹脂を主成分とする基材層である。基材層1の表
面には、第1被覆層2及び第2被覆層3の2層が
形成されている。これらは、太陽光の選択吸収能
を有している。 高密度ポリエチレン樹脂を主成分とする基材層
1は、その表面上に250μm以下の凹凸面4を設
けてある。第1被覆層2は、熱放射率の高い高密
度ポリエチレン樹脂を主成分とする基材層1の表
面を、低放射率の面にするための被覆層で、リー
フイング作用を示すメタリツク粉末5と、基材層
1の高密度ポリエチレン樹脂との良好な接着を得
るためのバインダーとしての塩素化ポリエチレン
変性アルキツド樹脂6を含む。第2被覆層3は、
太陽光の選択吸収能を有する被覆層で、赤外線領
域で比較的透過性が良く、第1被覆層2との接着
性が良好なバインダー7と、太陽光を良く吸収
し、赤外線には比較的透過性が良い酸化物または
複合酸化物8から成る顔料より形成され、5μm
を越えない範囲の被覆厚に形成される。 第1被覆層2及び第2被覆層3からなる被覆系
の作用を以下に説明する。a面側は太陽光受光
面、b面側は熱媒である。Aはこの太陽熱集熱板
表面に入射する太陽光を示す。太陽光Aは第2被
覆層3で吸収され、熱に変換される。変換された
熱は第1被覆層2、基材層1を熱伝導して、熱媒
b面側へと伝達される。他方、表面からの輻射損
失に関しては、第2被覆層3が赤外線に十分透過
性があるため、第1被覆層2のメタリツク粉末5
の性質により支配されるので、低放射率となり、
基材層1上に十分な選択吸収能を付与することが
できる。 基材層1の材質である高密度ポリエチレン樹脂
と、第1被覆層2との接着に関しては、従来極め
て接着が困難であつたが、塩素化ポリエチレン変
性アルキツド樹脂6を用いることで解消した。接
着の困難なポリエチレン樹脂との接着に関して、
塩素化ポリエチレン樹脂を用いるという技術は、
インキ等で実用化されているが、その多くは溶液
法で製造した比較的低分子量(分子量数千)で塩
素含量66%以上に高塩素化したものであり、低中
圧ポリエチレン樹脂に対する接着性は良好である
が、高密度ポリエチレン樹脂に対する密着性には
問題があつた。本実施例では水性懸濁法により製
造された分子量数万〜10数万で塩素含量30〜50%
の塩素化ポリエチレン樹脂とアルキツド樹脂を混
合した塩素化ポリエチレン変性アルキツド樹脂を
用いた。この塩素化ポリエチレン変性アルキツド
樹脂6は、塩素含量の程度が低いため、メタリツ
ク粉末5のリーフイング性を損なうことが少な
い。又、分子量が大きく、高密度ポリエチレン樹
脂との構造の類似部分がより多いため、良好な接
着性を有している。 又、第1被覆層2の密着性を十分よくしなが
ら、メタリツク粉末5のリーフイング性を保持す
るため、塩素化ポリエチレン変性アルキツド樹脂
6にエポキシ樹脂を添加した。エポキシ樹脂は、
メタリツク粉末5のリーフイング性を良好に保持
したまま、メタリツク粉末5自体を第1被覆層2
中に安定して接着する。 メタリツク粉末5としては、銅、アルミニウム
などのリーフイング性のある金属が適用可能であ
るが、本実施例では粒子の荒いアルミニウム粉を
用いた。特別な基材の処理を行なわない場合のメ
タリツク粉末5の配合比としては、5〜40wt%
の範囲で用いるのが良い。望ましくは、10〜
25wt%の範囲が最適のリーフイング特性と密着
性を与える。 又、第1被覆層2により赤外線放射率の低い表
面を得る場合には、メタリツク粉末5の配合率は
高ければ高い程よい。それに対して、基材層1と
の密着に関しては、逆にメタリツク粉末5の配合
率を高くすると密着性が悪くなる。これを解消す
るために、高密度ポリエチレン樹脂の基材層1の
表面に、平均250μm以下の微小な凹凸面4を形
成すると、接着面積が増加し、接着力が強くなる
が、この強くなる分だけメタリツク粉末5の配合
量を増加させたので、密着性を低下させずに放射
率を低下させることができた。第1被覆層2が形
成されると、金属とほぼ同等な低放射率の面が実
現するため、この第1被覆層2の上に、従来金属
面だけに適用されてきた、太陽光の選択吸収能を
有する第2被覆層3を設けることができる。 第2被覆層3としては、Fe、Mn、Cu、Cr、
Ni、Coの群から選択した1種以上の酸化物また
は複合酸化物8と、アクリル樹脂、フツソ樹脂、
ウレタン樹脂、アルキツド樹脂の群から選択した
1種以上の合成樹脂から成るバインダー7を主成
分とした。 上記金属の酸化物または複合酸化物8から成る
顔料は、赤外線吸収がほとんどなく、良好な太陽
光吸収能を有する。これらの酸化物または複合酸
化物8は0.01〜0.5μmの粒径範囲のものを用い
た。この粒径の場合には、太陽光を良好に散乱吸
収する効果が顕著である。アクリル樹脂、フツソ
樹脂、ウレタン樹脂、アルキツド樹脂は、いずれ
も第1被覆層2との良好な密着性を実現する。第
2被覆層3の被覆厚としてはあまり厚すぎると太
陽光の選択吸収能が悪くなるので5μmを越えな
い範囲とした。 以下、各被覆層に使用した素材の評価結果を示
す。 高密度ポリエチレン樹脂(但し、1.5wt%のカ
ーボンブラツクを含有)からなり、95mm×190mm
×10mmの寸法の板をテストピースとして用いた。
これは、内部が中空となつており、ブロー成型に
て、成型したものである。このテストピースに関
して、表裏を95mm×95mmの4つのゾーンに分け、
ブロー成型の金型に対して、40、60、80、及び
100メツシユの各粒度でサンドブラストした金型
を用いて、表裏の4つのゾーンに各々微小の凹凸
が形成される状態で成型した。走査型電子顕微鏡
にて、表面の凹凸を評価した所、40メツシユで
350μm、60メツシユで250μm、80メツシユで
180μm、100メツシユで150μm平均の凹凸面が形
成された。
INDUSTRIAL APPLICATION FIELD The present invention relates to a solar heat collector plate for a solar heat collector as a household water heater. Conventional structure and problems Conventional plastic solar heat collector plates are manufactured by blow molding a high-density polyethylene resin filled with carbon black, etc., but the surface has a selective absorption capacity for sunlight. I was bored. Further, as a means of achieving selective absorption ability on this surface, there was a method of painting, but the high density polyethylene resin of the base material layer had a large non-adhesive property, and sufficient adhesion could not be obtained. Purpose of the Invention The present invention provides a solar heat collecting plate in which a coating layer is provided on a base layer of high-density polyethylene resin, which increases the adhesion with high-density polyethylene resin, is inexpensive, and has the ability to selectively absorb sunlight. The purpose is to provide Structure of the Invention In order to achieve the above object, the present invention provides a surface layer of a base material layer mainly composed of high-density polyethylene resin.
On this base material layer, as an uneven surface of 250 μm or less,
It is provided with a coating layer that has the ability to selectively absorb sunlight. Description of Examples Examples of the present invention will be described below. The figure shows 3
Two layers are shown, and 1 is a base material layer whose main component is high-density polyethylene resin. Two layers, a first coating layer 2 and a second coating layer 3, are formed on the surface of the base layer 1. These have the ability to selectively absorb sunlight. The base material layer 1 mainly composed of high-density polyethylene resin has an uneven surface 4 of 250 μm or less on its surface. The first coating layer 2 is a coating layer for making the surface of the base material layer 1, which is mainly made of high-density polyethylene resin with a high thermal emissivity, into a low-emissivity surface, and is made of metallic powder 5 that exhibits a leafing effect. and a chlorinated polyethylene-modified alkyd resin 6 as a binder for obtaining good adhesion with the high-density polyethylene resin of the base material layer 1. The second coating layer 3 is
The coating layer has the ability to selectively absorb sunlight, has relatively good transparency in the infrared region, and has good adhesion to the first coating layer 2. Made from a pigment made of oxide or composite oxide 8 with good transparency, 5μm
The coating thickness is formed within a range not exceeding . The operation of the coating system consisting of the first coating layer 2 and the second coating layer 3 will be explained below. The a-plane side is a sunlight receiving surface, and the b-plane side is a heat medium. A indicates sunlight incident on the surface of this solar heat collector plate. Sunlight A is absorbed by the second coating layer 3 and converted into heat. The converted heat is thermally conducted through the first coating layer 2 and the base material layer 1, and is transferred to the heat medium b side. On the other hand, regarding radiation loss from the surface, since the second coating layer 3 is sufficiently transparent to infrared rays, the metallic powder 5 of the first coating layer 2
Since it is dominated by the properties of
Sufficient selective absorption ability can be provided on the base material layer 1. Conventionally, adhesion between the high-density polyethylene resin, which is the material of the base layer 1, and the first coating layer 2 was extremely difficult, but this problem was solved by using the chlorinated polyethylene-modified alkyd resin 6. Regarding adhesion with polyethylene resin, which is difficult to adhere to,
The technology of using chlorinated polyethylene resin is
It has been put into practical use as ink, etc., but most of them are relatively low molecular weight (molecular weight in the thousands) produced by a solution method and highly chlorinated with a chlorine content of 66% or more, and have poor adhesion to low-medium pressure polyethylene resin. was good, but there was a problem with the adhesion to high-density polyethylene resin. In this example, the molecular weight was tens of thousands to tens of thousands and the chlorine content was 30 to 50%, manufactured by an aqueous suspension method.
A chlorinated polyethylene modified alkyd resin, which is a mixture of chlorinated polyethylene resin and alkyd resin, was used. Since this chlorinated polyethylene modified alkyd resin 6 has a low chlorine content, the leafing properties of the metallic powder 5 are hardly impaired. Furthermore, since it has a large molecular weight and more structural similarities with high-density polyethylene resin, it has good adhesive properties. Further, in order to maintain the leafing properties of the metallic powder 5 while sufficiently improving the adhesion of the first coating layer 2, an epoxy resin was added to the chlorinated polyethylene modified alkyd resin 6. Epoxy resin is
The metallic powder 5 itself is coated in the first coating layer 2 while maintaining good leafing properties of the metallic powder 5.
Adheres stably inside. As the metallic powder 5, metals with leafing properties such as copper and aluminum can be used, but in this embodiment, coarse-grained aluminum powder was used. The blending ratio of metallic powder 5 when no special treatment is performed on the base material is 5 to 40 wt%.
It is best to use it within the range of Preferably 10~
A range of 25wt% provides optimal leafing properties and adhesion. Further, in order to obtain a surface with low infrared emissivity by the first coating layer 2, the higher the blending ratio of the metallic powder 5, the better. On the other hand, in terms of adhesion to the base material layer 1, if the blending ratio of the metallic powder 5 is increased, the adhesion becomes worse. In order to solve this problem, if a minute uneven surface 4 with an average size of 250 μm or less is formed on the surface of the base layer 1 made of high-density polyethylene resin, the bonding area will increase and the bonding force will become stronger. Since the blending amount of metallic powder 5 was increased by the same amount, the emissivity could be lowered without lowering the adhesion. When the first coating layer 2 is formed, a surface with a low emissivity almost equivalent to that of metal is realized. A second covering layer 3 having absorption capacity can be provided. The second coating layer 3 includes Fe, Mn, Cu, Cr,
One or more oxides or composite oxides 8 selected from the group of Ni and Co, acrylic resin, fluorine resin,
The main component is a binder 7 made of one or more synthetic resins selected from the group of urethane resins and alkyd resins. The pigment made of the metal oxide or composite oxide 8 has almost no infrared absorption and has good sunlight absorption ability. These oxides or composite oxides 8 used had particle sizes ranging from 0.01 to 0.5 μm. In the case of this particle size, the effect of scattering and absorbing sunlight well is remarkable. Acrylic resin, fluorine resin, urethane resin, and alkyd resin all achieve good adhesion with the first coating layer 2. The coating thickness of the second coating layer 3 was set within a range of not exceeding 5 μm, since if it was too thick, the selective absorption ability of sunlight would deteriorate. The evaluation results of the materials used for each coating layer are shown below. Made of high-density polyethylene resin (contains 1.5wt% carbon black), 95mm x 190mm
A plate with dimensions of ×10 mm was used as a test piece.
This is hollow inside and was molded by blow molding. Regarding this test piece, we divided the front and back into four zones of 95 mm x 95 mm.
For blow molding molds, 40, 60, 80, and
Using a sandblasted mold with a grain size of 100 mesh, molding was performed with minute irregularities formed in each of the four zones on the front and back sides. When the surface unevenness was evaluated using a scanning electron microscope, it was determined that the surface roughness was 40 mesh.
350μm, 60 mesh, 250μm, 80 mesh
An uneven surface with an average of 150 μm was formed with 180 μm and 100 meshes.

【表】【table】

【表】 前記基材層1上に表1に示した配合の塗料をボ
ールミルで1時間分散調合して、基材層1上に約
10〜20μmの被覆厚にて塗布し、60℃で30分間乾
燥させた。この第1被覆層2についての、特性の
評価結果を表2に示す。表中の密着性テストは、
セロテープ剥離試験を実施したもので、×は剥離、
△は点状の剥離が発生したことを示す。
[Table] The paint having the composition shown in Table 1 was dispersed and prepared on the base layer 1 for 1 hour using a ball mill, and then the paint was coated on the base layer 1 with approx.
A coating thickness of 10-20 μm was applied and dried at 60° C. for 30 minutes. Table 2 shows the evaluation results of the characteristics of this first coating layer 2. The adhesion test in the table is
A cellophane tape peeling test was carried out, where × indicates peeling,
△ indicates that point-like peeling occurred.

【表】 次に同じ各被覆層の上に、以下に示す配合の上
塗り塗料から成る第2被覆層3を被覆した。塗料
は、ボールミルにて、24時間分散調合した後、硬
化剤を加え、約2倍の溶剤にて希釈し、約1.5μm
の被覆厚にて、表2に示す被覆の上に塗布し、60
℃にて、30分間乾燥させたものを表3に示す。 (1) 顔 料:大日精化工業(株)「ダイピロキサイド
カラー#9550−F」(商品名)50重量部を使用。 (2) 合成樹脂:旭硝子(株)「ルミフロンLD−200」
(商品名)100重量部を使用。 (3) 溶 剤:「メチルイソブチルケトン:キシレ
ン=1:1」200重量部を使用。 (4) 硬化剤:日本ポリウレタン工業(株)「コロネー
トEH」(商品名)14.8重量部を使用。
[Table] Next, on each of the same coating layers, a second coating layer 3 consisting of a top coat of the composition shown below was coated. After dispersing and mixing the paint in a ball mill for 24 hours, a curing agent was added and diluted with approximately twice the amount of solvent, resulting in a thickness of approximately 1.5 μm.
Coated on the coating shown in Table 2 at a coating thickness of 60
Table 3 shows the results after drying at ℃ for 30 minutes. (1) Pigment: 50 parts by weight of "Dipyroxide Color #9550-F" (trade name) manufactured by Dainichiseika Chemical Co., Ltd. was used. (2) Synthetic resin: Asahi Glass Co., Ltd. “Lumiflon LD-200”
(Product name) Use 100 parts by weight. (3) Solvent: 200 parts by weight of "methyl isobutyl ketone:xylene = 1:1" was used. (4) Hardening agent: 14.8 parts by weight of "Coronate EH" (trade name) manufactured by Nippon Polyurethane Industries Co., Ltd. was used.

【表】 表3の結果を見ると、表2と比較して、一部密
着性が改善されているが、これは第2被覆層3の
バインダー7が第1被覆層2内にも入り込んで密
着性の改善に寄与したものである。 尚、自然循環式太陽熱温水器で、シミユレーシ
ヨン評価した所、無処理のプラスチツク製の太陽
熱集熱板を用いた場合と比較して、集熱効率が約
5%向上し、年間集熱量においても、約5%集熱
量が増加するという結果を得た。 又、前記塩素化ポリエチレン樹脂は分子量が大
きく、溶液粘度が高いため、やや他の樹脂との相
溶性で限界があるが、被覆系としての安定した物
性を実現するため、アクリル樹脂と混ぜて用いて
もよい。 以上のように、本実施例では、コスト的に有利
な塗装法により、従来接着が困難であつた高密度
ポリエチレン樹脂の基材層1上に、信頼性の高い
選択吸収能を有する被覆層を設けることができた
ので選択吸収処理のない従来のプラスチツク製の
太陽熱集熱板と比較して、集熱板表面からの放射
損失が半分以下に軽減化され、効率が向上した。 発明の効果 以上のように本発明によれば、次のような種々
のすぐれた効果を奏するものである。 太陽光の選択吸収性の付与により、太陽熱集
熱板の効率向上が達成される。 基材層の表面に250μm以下の凹凸面を設け
たので第1被覆層との密着性を悪化させること
なく、リーフイング性を高めることができる。 従来の太陽熱集熱板は、耐候劣化して、チヨ
ーキングを起こす欠点があつたが、本発明で
は、高耐候被覆の実施により、これが完全に防
止され、太陽熱集熱板として、高い信頼性が得
られる。 高価な金属板等を使用しないので安価な構成
が可能となる。 外気に直接触れる第2被覆層は、防錆性の良
い材質を使用できるので、海岸地帯等で使用し
ても、錆の発生がなく、優れた耐久性が期待で
きる。
[Table] Looking at the results in Table 3, the adhesion is partially improved compared to Table 2, but this is due to the binder 7 of the second coating layer 3 penetrating into the first coating layer 2. This contributed to improved adhesion. In addition, a simulation evaluation of a natural circulation solar water heater showed that the heat collection efficiency was improved by approximately 5% compared to using an untreated plastic solar heat collection plate, and the annual heat collection amount was also approximately 5% higher. The result was that the amount of heat collected increased by 5%. In addition, the above-mentioned chlorinated polyethylene resin has a large molecular weight and high solution viscosity, so its compatibility with other resins is somewhat limited, but in order to achieve stable physical properties as a coating system, it can be used by mixing it with acrylic resin. It's okay. As described above, in this example, by using a cost-effective coating method, a coating layer with highly reliable selective absorption ability was applied to the base material layer 1 of high-density polyethylene resin, which was difficult to adhere to in the past. Compared to conventional plastic solar heat collecting plates without selective absorption treatment, the radiation loss from the heat collecting plate surface was reduced by more than half, improving efficiency. Effects of the Invention As described above, the present invention provides the following various excellent effects. Improving the efficiency of the solar heat collector plate is achieved by imparting selective absorption of sunlight. Since the surface of the base layer is provided with an uneven surface of 250 μm or less, leafing properties can be improved without deteriorating the adhesion with the first coating layer. Conventional solar heat collecting plates had the disadvantage of weather resistance deterioration and tyoke, but with the present invention, this problem is completely prevented by applying a highly weather resistant coating, resulting in high reliability as a solar heat collecting plate. It will be done. Since expensive metal plates and the like are not used, an inexpensive configuration is possible. The second coating layer, which is in direct contact with the outside air, can be made of a material with good rust prevention properties, so even when used in coastal areas, it will not rust and excellent durability can be expected.

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

図面は、本発明の一実施例を示す拡大断面図で
ある。 1……基材層、2……第1被覆層、3……第2
被覆層、4……凹凸面、5……メタリツク粉末、
6……塩素化ポリエチレン変性アルキツド樹脂、
7……バインダー、8……酸化物または複合酸化
物。
The drawing is an enlarged sectional view showing one embodiment of the present invention. 1... Base material layer, 2... First coating layer, 3... Second
Covering layer, 4... Uneven surface, 5... Metallic powder,
6... Chlorinated polyethylene modified alkyd resin,
7... Binder, 8... Oxide or composite oxide.

Claims (1)

【特許請求の範囲】[Claims] 1 高密度ポリエチレン樹脂を主成分とする基材
層に、250μm以下の凹凸を表面に形成した上に
メタリツク粉末及び塩素化ポリエチレン変性アル
キツド樹脂を含む第1被覆層と太陽光の選択吸収
能を有する第2被覆層とを形成して成る太陽熱集
熱板。
1 A base material layer whose main component is high-density polyethylene resin, with irregularities of 250 μm or less formed on the surface, and a first coating layer containing metallic powder and chlorinated polyethylene-modified alkyd resin, which has the ability to selectively absorb sunlight. A solar heat collecting plate formed with a second coating layer.
JP57211560A 1982-08-18 1982-12-01 solar heat collector plate Granted JPS59100362A (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP57211560A JPS59100362A (en) 1982-12-01 1982-12-01 solar heat collector plate
AU18846/83A AU1884683A (en) 1982-08-18 1983-08-16 Solar heat collector
US06/606,773 US4556048A (en) 1982-08-18 1983-08-16 Solar heat collector
PCT/JP1983/000268 WO1984000804A1 (en) 1982-08-18 1983-08-16 Solar heat collector

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57211560A JPS59100362A (en) 1982-12-01 1982-12-01 solar heat collector plate

Publications (2)

Publication Number Publication Date
JPS59100362A JPS59100362A (en) 1984-06-09
JPS6410752B2 true JPS6410752B2 (en) 1989-02-22

Family

ID=16607815

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57211560A Granted JPS59100362A (en) 1982-08-18 1982-12-01 solar heat collector plate

Country Status (1)

Country Link
JP (1) JPS59100362A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62146268U (en) * 1986-02-27 1987-09-16
US8062738B2 (en) 2007-09-07 2011-11-22 Samsung Electronics Co., Ltd. Heat transfer medium and heat transfer method using the same

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BR7800749A (en) * 1977-02-09 1978-11-28 Dornier System Gmbh PROCESS FOR THE MANUFACTURE OF SELECTIVELY ABSORBENT SURFACES

Also Published As

Publication number Publication date
JPS59100362A (en) 1984-06-09

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