JPS59100362A - Solar heat collecting plate - Google Patents

Solar heat collecting plate

Info

Publication number
JPS59100362A
JPS59100362A JP57211560A JP21156082A JPS59100362A JP S59100362 A JPS59100362 A JP S59100362A JP 57211560 A JP57211560 A JP 57211560A JP 21156082 A JP21156082 A JP 21156082A JP S59100362 A JPS59100362 A JP S59100362A
Authority
JP
Japan
Prior art keywords
coating layer
base material
material layer
sunlight
density polyethylene
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP57211560A
Other languages
Japanese (ja)
Other versions
JPS6410752B2 (en
Inventor
Masao Maki
正雄 牧
Yu Fukuda
祐 福田
Yasunori Kaneko
金子 康典
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 PCT/JP1983/000268 priority patent/WO1984000804A1/en
Priority to AU18846/83A priority patent/AU1884683A/en
Priority to US06/606,773 priority patent/US4556048A/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)

Abstract

PURPOSE:To form a solar heat collecting plate on a base material layer of high density polyethylene resin to be obtained by providing a coating layer, which is highly adhesive, inexpensive and having selective absorbing capacity of the sunlight, on the base material layer made of high density polyethylene resin, by providing the coating layer having the selective absorbing capacity of the sunlight by making the surface of the base material layer into an uneven face of less than 250mum. CONSTITUTION:The surface of a base material layer 1 having high density polyethylene resin for its main ingredient is provided with an uneven face 4 of less than 250mum. A first coating layer 2 contains metallic powder 5 showing roofing action and chrolinated polyethylene denatured alkid resin 6 as a binder for obtaining favorable adhesion with the high density polyethylene resin of the base material layer 1, a second coating layer 3 is the coating layer having selective absorbing capacity of the sunlight, permeability is comparatively favorable in a infrared ray sphere and is formed by a pigment consisting of the binder 7 whose adhesiveness with the first coating layer 2 is favorable and an oxide or a composite oxide 8 which absorbs the sunlight favorably and permeability to an infrared ray is comparatively favorable.

Description

【発明の詳細な説明】 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。
DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a solar heat collector plate for a solar heat collector as a household water heater.

従来例の構成とその問題点 従来のプラスチッ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ック等を充填し、ブロー成
型モ製造されているか、その表面には太陽光の選択吸収
能がなかった。
Conventional structure and problems Conventional plastic solar heat collector plates are manufactured by blow molding high-density polyethylene resin filled with carbon black, etc., or the surface has a selective absorption ability for sunlight. There wasn't.

また、この表面に選択吸収能を実現する手段として、塗
装による手段かあったが、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
か得られなかった。
Also, as a means of achieving selective absorption ability on this surface, there was a method of painting, but sufficient adhesion could not be obtained due to the high non-adhesiveness of the high-density polyethylene resin of the base material layer.

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。
Purpose of the invention The present invention improves adhesion to high density polyethylene resin,
The object of the present invention is to provide a solar heat collecting plate which is inexpensive and has a coating layer having the ability to selectively absorb sunlight on a base layer of high-density polyethylene resin.

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。
Structure of the Invention In order to achieve the above object, the present invention provides a base material layer whose main component is a high-density polyethylene resin, with an uneven surface of 250 μm or less, and which has a selective absorption ability for sunlight on this base material layer. A coating layer having the following properties is provided.

実施例の説明 以上、木発明の実施例を説1υjする。図には、3つの
hか示されており、(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)の表向には、
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
DESCRIPTION OF EMBODIMENTS Above, embodiments of the tree invention will be explained. In the figure, three h are shown, and (1) is a base material layer whose main component is high-density polyethylene resin. On the surface of the base layer (1),
Two layers are formed: a first coating layer (2) and a second coating layer (3). These have the ability to selectively absorb sunlight.

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す、下の凹凸面(4)を設け
である。第1被覆1fj4 (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
表向を、低放射率の面にするだめの被覆層で、リーフィ
ング作用を示すメタリック粉末(5)と、基材層(1)
の高密度ポリエチレン極脂との良好な接名を得るための
バインターとしての塩素化ポリエチレン変性アルキッド
樹脂(6)を含む。第2被榎肋(3)は、太陽光の選択
吸収fiしを有する被覆層で、赤外線領域で比較的透過
性か良く、第1被へ層(2)との接着性か良好なバイン
ダー(7)と、太1為光を良く吸収し、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1成
る顔料より形成さオ′1.5μn1を越えない範囲の被
覆厚に形成される。
The base material layer (1) mainly composed of high-density polyethylene resin was provided with a lower uneven surface (4) having a thickness of 250 μm on its surface. The first coating 1fj4 (2) is a coating layer that makes the surface of the base layer (1), which is mainly made of high-density polyethylene resin with a high thermal emissivity, a low-emissivity surface, and has a leafing effect. Metallic powder (5) shown and base material layer (1)
Contains chlorinated polyethylene modified alkyd resin (6) as a binder to obtain good contact with high density polyethylene super fat. The second coating layer (3) is a coating layer that selectively absorbs sunlight, has relatively good transparency in the infrared region, and has a binder ( 7) and a pigment consisting of an oxide or composite oxide (8) which absorbs light well and has relatively good transparency to infrared rays, and has a coating thickness not exceeding 1.5 μn1. is formed.

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Tlこ説明する。8面側は太陽光受光面、1
3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被葎層(3)で吸収
され、熱1こ変換される。変換された熱は第1被八層(
2)、基材層(1)を熱伝導して、熱媒l)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)か赤外線に十分透過性があるため、第1被
覆層(2)のメタリック粉末(5)の性質により支配さ
れるのて、低放射率となり、基材層ti+−t−tこ1
分な選択吸収能を付与するこ乏ができる。
The operation of the coating system consisting of the first coating layer (2) and the second coating layer (3) will now be explained. The 8th side is the sunlight receiving surface, 1
The third 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 seedling layer (3) and converted into 1 part of heat. The converted heat is transferred to the first 8th layer (
2) The heat is conducted through the base material layer (1) and transferred to the heat medium l) surface side. On the other hand, regarding radiation loss from the surface, the second
Since the coating layer (3) is sufficiently transparent to infrared rays, it has a low emissivity, which is controlled by the properties of the metallic powder (5) of the first coating layer (2), and the base material layer ti+-t-t This 1
Therefore, it is difficult to impart sufficient selective absorption capacity.

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
が困難であったが、塩素化ポリエチレン変性アルギツド
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1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昂(分子
石数千)で塩素3晴66%以上に高塩素化(、たもので
あり、低中圧ポリエチレン樹脂に対する接箔性は良好で
あるが、高密度ポリエチレン樹脂に対する密着性には問
題かぁ−)だ。本実施例では水性懸濁法により製造され
た分子(i数万〜10数力で塩素含−1130〜50%
の塩素化ポリエチレン樹脂とアルキンド樹脂を混合した
塩素化ポリエチレン変性アルキッド樹脂を用いた。この
3M素化ポリエチレン変性アルキッド樹脂(6)は、塩
素金属の程度が低いため、メタリック粉末(5)のリー
フィング性を損Is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かより
多いため、良好な接着性を有しでいる。
High-density polyethylene resin, which is the material of the base layer (1),
Regarding adhesion with the first coating layer (2), adhesion was extremely difficult in the past, but this was solved by using the chlorinated polyethylene modified algide resin (6). Regarding contact with polyethylene resin, which is difficult to adhere to, the technology of using chlorinated polyethylene resin has been put to practical use in inks, etc., but most of them are made using relatively low molecular weight compounds (thousands of molecular stones) manufactured by a solution method. ) and has a high chlorine concentration of 66% or more, and has good adhesion to low-medium pressure polyethylene resin, but there are problems with adhesion to high-density polyethylene resin. In this example, molecules manufactured by the aqueous suspension method (i.
A chlorinated polyethylene modified alkyd resin, which is a mixture of chlorinated polyethylene resin and alkyd resin, was used. Since this 3M bare polyethylene modified alkyd resin (6) has a low level of chlorine metal, it hardly impairs the leafing properties of the metallic powder (5). In addition, since the molecular weight is large and there are more structurally similar parts to that of high-density polyethylene resin, it has good adhesive properties.

又、第1被PA j* (2)の密着性を十分よくしな
がら、メタリック粉末(5)のリーフィング性を保持す
るため、塩素化ポリエチレン変性アルキッド極脂(6)
にエポキシ樹脂を添加した。エポキシ樹脂は、メタリッ
ク粉末(5)のリーフィング性を良好に保持したまま、
メタリック粉末(5)自体を第1被覆層(2)中に安定
して接着する。
In addition, in order to maintain the leafing properties of the metallic powder (5) while sufficiently improving the adhesion of the first PA j* (2), chlorinated polyethylene modified alkyd super fat (6) is added.
Epoxy resin was added to. The epoxy resin maintains good leafing properties of the metallic powder (5),
The metallic powder (5) itself stably adheres into the first covering layer (2).

メタリック粉末(5)としては、銅、アルミニウムなど
のり・−フインク性のある金執か適用可能であるか、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ック粉末(5)の
配合比と1〜では、5〜4 Q wt・%の範囲で用い
るのか良い。望ま(−<は、10〜25wt・%の範囲
か最適のリーフインク特性と密着性を与える。
As the metallic powder (5), it is possible to use metals with adhesive properties such as copper or aluminum, or in this example, coarse-grained aluminum powder was used. If the mixing ratio of metallic powder (5) is 1 to 1 when no special treatment is performed on the base material, it is best to use the metallic powder in a range of 5 to 4 Q wt.%. Desired (-< is in the range of 10 to 25 wt.% or gives optimum leaf ink properties and adhesion.

又、第J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、メタリック粉末(5)の配合率は高けれ
は高い程よい。それに対1−で、基材層(1)との密着
に関しては、逆にメタリック粉末(5)の配合率を篩く
すると密着性か悪くなる。2これを解消するために、高
密度ポリエチレン樹脂の基1層(1)の表面に、十−均
250μnl以”干の微小な凹凸面(4)を形成する古
、接着面積か増加し、接着力が強くなるか、この強くな
る分だけメタリック粉末(5)の配合量を増加させたの
で、密お性を低下させずに放射率を低ドさせることかで
きた。第1被覆層(2)か形成されると、金属とほぼ同
等な低放射率の面か実現するため、この第1被覆層(2
)の上に、従来金属面た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〜層(3)を設けることかで
きる。
Moreover, when obtaining a surface with low infrared emissivity by the J-th coating layer (2), the higher the blending ratio of the metallic powder (5), the better. On the other hand, with respect to the adhesion with the base material layer (1), conversely, if the blending ratio of the metallic powder (5) is reduced, the adhesion becomes worse. 2 In order to solve this problem, a fine uneven surface (4) of 250 μnl or more in size is formed on the surface of the base layer (1) of high-density polyethylene resin. By increasing the amount of metallic powder (5) in proportion to the strength of the force, it was possible to lower the emissivity without reducing the tightness.The first coating layer (2) ) is formed, this first coating layer (2
) can be provided with a second covering layer (3) having the ability to selectively absorb sunlight, which has conventionally been applied only to metal surfaces.

第2被覆層(3)としては、Fe、 Mn、 Cu、 
<2r。
The second coating layer (3) includes Fe, Mn, Cu,
<2r.

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、フッソ樹脂、ウレタ
ン樹脂、アルキッ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。
A binder (7) consisting of one or more oxides or composite oxides (8) selected from the group of Ni and Co and one or more synthetic resins selected from the group of acrylic resins, fluorocarbon resins, urethane resins, and alkyd resins. ) was the main component.

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.
01〜0.5μn)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、フッソ樹脂、ウレタン樹脂、ア
ルキッド樹脂は、いずれも第1被覆層(2)との良好な
密着性を実現する。
The pigment made of the metal oxide or composite oxide (8) has almost no infrared absorption and good sunlight absorption ability. These oxides or composite oxides (8) have 0.
Particles having a particle size range of 0.01 to 0.5 μn were used. In the case of this particle size, the effect of scattering and absorbing sunlight well is remarkable. Acrylic resin, fluorocarbon resin, urethane resin, and alkyd resin all achieve good adhesion with the first coating layer (2).

第2被覆@(3)の被覆厚としてはあまり厚すきると太
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。
The thickness of the second coating (3) was determined not to exceed 5 μm since the selective absorption ability of sunlight would deteriorate if it was too thick.

以下、各被覆層に使用した素材の評価結果を示す。The evaluation results of the materials used for each coating layer are shown below.

高密度ポリエチレン樹脂(但し、1,5wt  %のカ
ーボンブラックを含有)からなり、95mm×1g o
ram X 1011M+の寸法の板をテストピースと
して用いた。これは、内部が中空となっており、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、表裏ヲ95mm×95mm(D4ツ(DV’−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フラストした金
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。
Made of high density polyethylene resin (contains 1.5wt% carbon black), 95mm x 1g o
A board with dimensions of ram X 1011M+ was used as a test piece. This is hollow inside and was molded by blow molding. Regarding this test piece, the front and back sides are 95mm x 95mm (divided into D4 pieces (DV'-), and 40°60.80mm for the blow molding mold.
, and 100 mesh, using sand-frust molds with particle sizes of 100 and 100 mesh, and molding was carried out in a state in which minute irregularities were formed in each of the four zones on the front and back sides.

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゛ンシユで250μm1
80メツシユで180μm、100メ゛ンシユで150
μm平均の凹凸面か形成された。
When the surface unevenness was evaluated using a scanning electron microscope, it was found to be 40
350μm for mesh, 250μm for 60 mesh1
180μm for 80 mesh, 150 for 100 mesh
An uneven surface with a μm average was formed.

表1 第1被覆層の配合(重量部) 1 )T;!4洋アルミニウム(株) :アルペースト
「0100X」C商品名)を使用。
Table 1 Formula of first coating layer (parts by weight) 1) T;! 4-Yo Aluminum Co., Ltd.: Alpaste "0100X" C (trade name) was used.

2)は大阪曹達(株):エマルラツクス「P−35」(
商品名)を使用。
2) Osaka Soda Co., Ltd.: Emul Lux “P-35” (
Product name) is used.

3)は油化シェルエポキシ(株):エピコートr821
3J(商品名)を使用。
3) is Yuka Shell Epoxy Co., Ltd.: Epicoat R821
Uses 3J (product name).

4)は「トルエン」を使用。4) uses "toluene".

前記基材層(」)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°Cて30分間乾
燥させた。この第1被扱層(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、Xは剥離、△は点状の剥
離か発生したことを示す。
On the base material layer (1), a paint having the composition shown in Table 1 is dispersed and prepared in a ball mill for 1 hour, and the paint is coated on the base material layer (1) with a coating composition shown in Table 1.
A coating thickness of 20 μm was applied and dried at 60° C. for 30 minutes. Table 2 shows the evaluation results of the characteristics of this first treated layer (2). The adhesion test in the table was carried out by cellophane tape peeling test, where X indicates peeling and △ indicates that dotted peeling occurred.

表2 第1被覆層の評価結果 次に同し各被咎層の上に、以下に示す配合の上塗り塗料
から成る第2被扱層(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1.5f1111の被覆厚に
て、表2に示す被覆の上(こ塗布し、60°Cにて、3
0分間乾燥させたものを表3に示す。
Table 2 Evaluation results of the first coating layer Next, a second coating layer (3) consisting of a top coat of the composition shown below was coated on each of the same coating layers. After dispersing and blending the paint in a ball mill for 24 hours, a curing agent was added and diluted with approximately twice the amount of solvent. , at 60°C, 3
Table 3 shows the results after drying for 0 minutes.

+11顔   料:大日精化工業(株)1′ダイピロキ
サイドカラー09550−1”J(商品名)50重例部
を使用。
+11 pigment: Dainichiseika Chemical Co., Ltd. 1' Dipyroxide Color 09550-1''J (trade name) 50 parts.

(2)合成樹脂:旭硝子(株)[ルミフロン川−)−2
00J(商品名)100重廿1部を使用。
(2) Synthetic resin: Asahi Glass Co., Ltd. [Lumifron River-)-2
Use 1 part of 00J (product name) 100 weight.

(3)溶    剤: 「メチルインブチルケトン:キ
シレン−1:1−200重量部を使用。
(3) Solvent: ``Methyl in butyl ketone:xylene-1:1-200 parts by weight was used.

(4)硬 化 剤二 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。
(4) Curing agent 2 14.8 parts by weight of "Coronate EH" (trade name) manufactured by Nippon Polyurethane Industries Co., Ltd. was used.

表3の結果を見ると、表2と比較して、一部密名性か改
俣されているか、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4件の改
善に寄与したものである。
Looking at the results in Table 3, it appears that the binder (7) in the second coating layer (3) is partially hidden in the first coating layer (2) compared to Table 2. This also contributed to the improvement of the 4 cases of close contact.

尚、自然循環式太陽熱温水器で、シミュレーション評価
した所、無処理のプラスチック製の太陽熱集熱板を用い
た場合と比較して、集熱効率か約5%向」ニし、年間集
熱量においても、約り%集熱叶か増加するという結果を
得た。
In addition, a simulation evaluation of a natural circulation solar water heater showed that the heat collection efficiency was approximately 5% higher than when using an untreated plastic solar heat collection plate, and the annual heat collection amount was also lower. The result was that the heat collection capacity increased by approximately %.

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、やや池のわj脂との相溶性て限界
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。
Further, the chlorinated polyethylene resin has a large molecular weight,
Due to the high solution viscosity, there is a limit to its compatibility with Ike no Wajō fat, but in order to achieve stable physical properties as a coating system, it may be used in combination with an acrylic resin.

以」二のように、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っ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角
する被覆層を設けることかできたので選択吸収処理のな
い従来のプラスチッ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か半分り、下に軽減化され、効
率か向上した。
As described above, in this example, by using a cost-effective coating method, highly reliable selective absorption ability was achieved on the base material layer (1) of high-density polyethylene resin, which was difficult to adhere to in the past. Because we were able to provide a corner coating layer, compared to conventional plastic solar heat collection plates that do not have selective absorption treatment, the radiation loss from the heat collection plate surface is reduced by half, resulting in improved efficiency. Improved.

発明の効果 以上のように本発明によれは、次のような種々のすぐれ
た効果を奏するものである。
Effects of the Invention As described above, the present invention provides the following various excellent effects.

■ 太陽光の選択吸収性の伺与により、太陽熱集熱板の
効率向上が達成される。
■ Improved efficiency of solar heat collector plates can be achieved by selectively absorbing sunlight.

■ 基材層の表面に250μm11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
ーフィング性を高めることができる。
(2) Since the surface of the base layer is provided with an uneven surface of 250 μm11 or less, the leafing property can be improved without deteriorating the adhesion with the first coating layer.

■ 従来の太陽熱集熱板は、耐候劣化して、チョーキン
グを起こす欠点があったが、本発明では、高4候被覆の
実施により、これが完全に防止され0、太陽熱集熱板と
して、高い信頼性が得られる。
■ Conventional solar heat collecting plates had the drawback of deteriorating weather resistance and causing chalking, but with the present invention, this is completely prevented by implementing a high 4 weather coating, making it highly reliable as a solar heat collecting plate. You can get sex.

■ 高価な金属板等を使用しないので安価な構成か可能
となる。
■ Since expensive metal plates etc. are not used, an inexpensive configuration is possible.

■ 外気に直接触れるm2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
かなく、優れた耐久性か期待できる。
■ The m2 coating layer, which is in direct contact with the outside air, can be made of a material with good rust prevention properties, so even if used in coastal areas, it will not rust and can be expected to have excellent durability.

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

図面は、本発明の一実施例を示す拡大断面図である。 (月・・基材層、+21・・第1被務層、(3)・・・
第2被覆層、(4)・・凹凸部、(5)・・メタリック
粉末、(6)・・塩素化ポリエチレン変性アルキッド樹
脂、(7)・・・バインダー、(8)・・酸化物または
複合酸化物。 代理人 弁理士人 島 −公 手続補正書(方灼 1、事件の表示 昭和57年特許願順光211560  号2、発明の名
称 太陽熱集熱板 一一、、−’ 4、代理人 5補正命令又は拒絶理由通知の日イ\4昭和、8年3 
月29F〕 6 補正の対象 明細書中、発明の詳細な説明の欄 7、 補正の内容 明m書中、第9頁、第10頁、第12頁を91J紙の通
り補正する。(浄書番こつき内容器こ変更な・し) 表1 第1被&層の配合(重量部) 1)は東洋アルミニウム(株):アルペース)rolo
oXJ(商品名)を使用。 2)は大阪曹達(株):エマルラックスrP−35J(
商品名)を使用。 3)は油化シェルエポキシ(株):エピコー)r828
J(商品名)を使用。 4〕は「トルエン」を使用。 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被怪層(21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、Xは剥離、△は点状の剥離
が発生したことを示す。 表2 第1被覆層の評価結果 次に同し各波峰層の上に、以下番こ示す配合の上塗り塗
料から成る第2被&層(3+を被しした。塗料は、ボー
ルミル番こて、244時間分散調した後、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。
The drawing is an enlarged sectional view showing one embodiment of the present invention. (Moon: base material layer, +21: first working layer, (3)...
Second coating layer, (4)...Irregularities, (5)...Metallic powder, (6)...Chlorinated polyethylene modified alkyd resin, (7)...Binder, (8)...Oxide or composite oxide. Agent Patent attorney Shima - Public procedure amendment (Method 1, Case indication 1982 Patent application Junko 211560 No. 2, Title of invention Solar heat collecting plate 11, -' 4. Agent 5 Amendment order Or the day of notification of reasons for refusal \4 Showa, 3rd year of 8th year
Month 29F] 6 In the specification to be amended, column 7 of the detailed description of the invention and pages 9, 10, and 12 of the statement of contents of the amendment are amended as per paper 91J. (Engraving number: No change to the inner container.) Table 1: Composition of the first layer & layer (parts by weight) 1) is manufactured by Toyo Aluminum Co., Ltd.: Alpace) Rolo
Use oXJ (product name). 2) Osaka Soda Co., Ltd.: Emullux rP-35J (
Product name) is used. 3) is Yuka Shell Epoxy Co., Ltd.: Epicor) r828
Use J (product name). 4] uses “toluene”. On the base layer (1), a paint having the composition shown in Table 1 is dispersed and mixed in a ball mill for 1 hour to form a coating material on the base layer (1) for about 10 to 10 minutes.
It was applied to a coating thickness of 20 μm and dried at 60° C. for 30 minutes. Table 2 shows the evaluation results of the characteristics of this first covered layer (21).The adhesion test in the table was carried out using cellophane tape peeling test. Table 2 Evaluation results of the first coating layer Next, a second coating (3+) consisting of a top coat of the composition shown below was applied on each of the same wave ridge layers. After dispersing with a ball mill trowel for 244 hours, a curing agent was added, diluted with approximately twice the amount of solvent, and applied to a coating thickness of approximately 1.5 μm on the coating shown in Table 2, and heated at 60°C. Table 3 shows the results after drying for 30 minutes.

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
層と、この基材層」−に設けられ且つ太陽光の選択吸収
能を有する被覆層とを備え、前記基材層の表面を250
μn1以下の凹凸面とした太陽熱集熱板。 (21被覆層として、メタリック粉末に対し、バインタ
ーとして塩素化ポリエヂレン変性アルキッド樹脂を含む
第1被覆層と、太陽光の選択吸収能を有する第2被覆層
との2脂とした特許請求の範囲第1項記載の太陽熱集熱
板。
(1) A base material layer containing high-density polyethylene resin as a main component, and a coating layer provided on this base material layer and having a selective absorption ability of sunlight, the surface of the base material layer being 250%
A solar heat collector plate with an uneven surface of μn1 or less. (21) The first coating layer contains a chlorinated polyethylene-modified alkyd resin as a binder for the metallic powder as the coating layer, and the second coating layer has the ability to selectively absorb sunlight. The solar heat collecting plate according to item 1.
JP57211560A 1982-08-18 1982-12-01 Solar heat collecting 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 collecting plate
PCT/JP1983/000268 WO1984000804A1 (en) 1982-08-18 1983-08-16 Solar heat collector
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

Applications Claiming Priority (1)

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

Publications (2)

Publication Number Publication Date
JPS59100362A true JPS59100362A (en) 1984-06-09
JPS6410752B2 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 collecting plate

Country Status (1)

Country Link
JP (1) JPS59100362A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62146268U (en) * 1986-02-27 1987-09-16
JP2009062538A (en) * 2007-09-07 2009-03-26 Samsung Electronics Co Ltd Heat transfer medium and heat transfer method utilizing the same

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5398533A (en) * 1977-02-09 1978-08-29 Dornier System Gmbh Selective solar absorption surface layer

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5398533A (en) * 1977-02-09 1978-08-29 Dornier System Gmbh Selective solar absorption surface layer

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62146268U (en) * 1986-02-27 1987-09-16
JP2009062538A (en) * 2007-09-07 2009-03-26 Samsung Electronics Co Ltd Heat transfer medium and heat transfer method utilizing the same
US8945687B2 (en) 2007-09-07 2015-02-03 Samsung Electronics Co., Ltd. Heat transfer medium and heat transfer method using the same

Also Published As

Publication number Publication date
JPS6410752B2 (en) 1989-02-22

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