JPS6337862B2 - - Google Patents
Info
- Publication number
- JPS6337862B2 JPS6337862B2 JP57078927A JP7892782A JPS6337862B2 JP S6337862 B2 JPS6337862 B2 JP S6337862B2 JP 57078927 A JP57078927 A JP 57078927A JP 7892782 A JP7892782 A JP 7892782A JP S6337862 B2 JPS6337862 B2 JP S6337862B2
- Authority
- JP
- Japan
- Prior art keywords
- paint
- coating
- selective absorption
- absorption
- film
- 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
Links
- 238000010521 absorption reaction Methods 0.000 claims description 25
- 238000000576 coating method Methods 0.000 claims description 24
- 239000011248 coating agent Substances 0.000 claims description 23
- 239000003973 paint Substances 0.000 claims description 18
- 229920005989 resin Polymers 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 9
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- 229920001577 copolymer Polymers 0.000 claims description 6
- 239000007787 solid Substances 0.000 claims description 6
- 229910052804 chromium Inorganic materials 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 229910052742 iron Inorganic materials 0.000 claims description 4
- 229910052748 manganese Inorganic materials 0.000 claims description 4
- 229920002050 silicone resin Polymers 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- 239000002131 composite material Substances 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 239000010408 film Substances 0.000 description 23
- 239000000203 mixture Substances 0.000 description 6
- 239000000049 pigment Substances 0.000 description 5
- 230000007547 defect Effects 0.000 description 4
- 238000010790 dilution Methods 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000010422 painting Methods 0.000 description 4
- 239000011651 chromium Substances 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- -1 etc. Polymers 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- 229910020599 Co 3 O 4 Inorganic materials 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- ALKZAGKDWUSJED-UHFFFAOYSA-N dinuclear copper ion Chemical compound [Cu].[Cu] ALKZAGKDWUSJED-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229940056932 lead sulfide Drugs 0.000 description 1
- 229910052981 lead sulfide Inorganic materials 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S70/00—Details of absorbing elements
- F24S70/20—Details of absorbing elements characterised by absorbing coatings; characterised by surface treatment for increasing absorption
- F24S70/25—Coatings made of metallic material
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F24—HEATING; RANGES; VENTILATING
- F24S—SOLAR HEAT COLLECTORS; SOLAR HEAT SYSTEMS
- F24S70/00—Details of absorbing elements
- F24S70/20—Details of absorbing elements characterised by absorbing coatings; characterised by surface treatment for increasing absorption
- F24S70/225—Details of absorbing elements characterised by absorbing coatings; characterised by surface treatment for increasing absorption for spectrally selective absorption
-
- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/40—Solar thermal energy, e.g. solar towers
Landscapes
- Engineering & Computer Science (AREA)
- Physics & Mathematics (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)
- Spectroscopy & Molecular Physics (AREA)
Description
本発明は、太陽熱の集熱器に適用され、かつそ
の表面上に太陽熱の選択吸収性を付与することが
できる太陽熱の選択吸収性塗膜の形成方法に関す
るもので、特に高性能の選択吸収塗膜を実現する
方法を提供するものである。
一般に太陽熱集熱器の効率向上に寄与する技術
としては、選択吸収膜を形成する技術があるが、
この場合、大きな面積の塗布の適用性に優れ、か
つコストの安価な塗装が注目されている。この塗
装により選択吸収性を実現するためには、その構
成系の組み合わせが重要である。
従来からこの組み合わせとして、硫化鉛微粉末
をシリコーン樹脂中に分散した塗料を始めとし
て、銅化銅、二酸化マンガン、酸化コバルトなど
と、アクリルメラミン系、ビニル系、シリコーン
系などの樹脂との組み合わせが提案されている。
塗料法で、選択吸収特性を高めるためのポイント
は、高くなりがちな放射率を如何にして、改善す
るかにある。
従来の組み合わせ系で総合的にバランスのとれ
た構成となつているものにおいては、太陽光吸収
率αが0.93〜0.94、赤外線放射率εが0.4〜0.5(但
し、ステンレスが基材の場合)の選択吸収性を有
するのが水準であつた。この水準は、塗装以外の
選択吸収膜と比較すると放射率が高い水準にあ
る。
従来の構成系で、放射率を改善しようとすれ
ば、膜厚を薄く構成できれば良いが、膜厚を薄く
安定して均一に塗装することは非常に困難であ
り、また膜厚を薄くすれば、ピンホール等の欠陥
も増え、塗膜物性が悪くなる上に、太陽光吸収率
も低下してしまうという欠点があつた。
本発明は、上記従来の欠点に鑑み、塗膜にピン
ホールなどの欠陥を生ずることを極力防止して、
塗装作業性を良好にし、かつ優れた選択吸収性を
実現する方法を提供することを目的とするもので
ある。
上記目的を達成するために、本発明は、カルボ
ン酸アミド共重合体と、Fe、Mn、Cu、Cr、Co、
Niの群から選択した1種以上の元素を含む酸化
物または複合酸化物と、低分子量4フツ化エチレ
ン樹脂を主成分とする溶剤系塗料を用いて、塗料
中の固形分率を重量分率で10wt%以下として、
アミノ変性シリコーン樹脂を添加した状態にて、
集熱面上に塗布し、その後、加熱硬化させるよう
にしたものである。
上記カルボン酸アミド共重合体は、結合剤であ
つて、金属などの集熱面素地上に膜を作るための
ものである。すなわち、素地との密着、さらに
は、他の塗膜構成要素を相互に接着するためのも
のである。
またFe、Mn、Cu、Cr、Co、Niの群から選択
した1種以上の元素を含む酸化物または、複合酸
化物は、太陽光を吸収するためのもので、赤外線
の吸収が少ない黒色顔料として用いている。
上記赤外線の吸収に関しては、いずれの樹脂と
も、かなりの吸収は避けられないが、カルボン酸
アミド共重合体は、比較的赤外線の吸収が少ない
樹脂である。
また低分子量4フツ化エチレン樹脂は、塗膜物
性を改善するために用いているもので、この樹脂
の採用により、耐食性や耐摩耗性、耐衝撃性、耐
熱性などが改善される。また1〜2μmの近赤外
線領域の吸収を改善する目的にもこの低分子量4
フツ化エチレン樹脂は寄与する。
そしてまた集熱面の放射率を低くするために
は、表面の放射率が低い素材を用いて、これを利
用する。また素材の低い放射率を損なわないため
には、形成する塗膜は極力薄板であることが望ま
しい。薄膜の塗膜を安定して均一に形成するた
め、塗料中の固形分量は少ない状態で塗装するの
が良い。すなわち、塗料中の固形分率を重量分率
で10wt%以下としたのは、このためで、例えば
固形分率が重量分率でawt%とすれば、塗料の希
釈度は約100/aとなり、仮に5wt%とした場合、希
釈度は約20倍で、20μmのウエツト膜厚で1μmの
ドライ膜厚が得られる計算となる。このようにす
ることにより、安定した薄膜の形成が可能とな
る。
従来の塗料では、このような希釈度の高い状態
では、顔料と樹脂が分離したりして、ピンホール
等の種々の塗膜欠陥が生じやすいのであるが、本
発明の場合には、アミノ変性シリコーン樹脂を含
み、安定した表面張力状態が保持されているた
め、塗膜欠陥の発生の懸念がなく、安定した塗装
作業が可能となる。
このようにして塗布した後、通常の焼付け炉で
加熱硬化させれば、容易に性能の優れた選択吸収
塗膜が形成される。
本発明におけるカルボン酸アミド共重合体は、
望ましくは、アクリルアミドか、メタアクリルア
ミドなどのα,βモノエチレン性不飽和カルボン
酸、アクリル酸アルキルエステルなどを主成分と
する共重合体の適用が望ましい。これらの樹脂
は、耐候性、耐熱性、耐食性、硬度、薄塗り性な
どの面で優れた特性を有しているためである。
顔料は、Fe、Mn、Cu、Cr、Co、Niの群から
選択したFe3O4、MnO2、CuO、Co3O4、NiOな
どの顔料単独もしくは混合物、特に、Fe2O3−
MnO2・CuO、あるいはCuO−Cr2O3などの混合
物が、赤外域の透明性と、太陽光吸収域の吸収性
の面で特に良好である。また、これらの顔料に関
しては、特にその粒径が重要な要因であり、0.01
〜0.5μmの粒径範囲が、選択吸収性、特に光散乱
の観点で望ましい。
以下、本発明の実施例を中心として、効果を説
明する。なお、選択吸収性の評価は以下の方法で
行なつた。吸収率αの評価は、島津製作所製
MPS−5000型自記分光光度計(入射角8゜、積分
球反射装置付き)を用いて、波長0.3〜2.0μmの
間での測定値から、6000〓の黒体の輻射率に対し
て計算した。また放射率(ε)の評価は、
DEVICES & SERVICES COMPANY社製D
andS AERD型放射率計を用いて直接評価し
た。
実施例
テストピースとしては、70mm×150mm×0.3mmt
の寸法を有する新日鉄(株)製のステンレスYUS−
190(商品名)を用い、そして塗料は表1の配合で
調合した。この塗料は固形分が約34%の構成であ
る。この塗料を約1μmの膜厚の薄膜に塗装する
ために、塗料と同じ組成の溶剤で希釈した場合、
塗布面のムラ(ピンホール、うき)を生じること
なく、希釈できるのは、高々15%の領域である。
これを単なるスプレー塗装で塗装するのであれ
ば、もつと希釈を上げることも可能であるが、デ
イスクを用いた静電塗装で行なうのは困難であ
る。そこで、表1の塗料を15重量部、溶剤を85重
量部として、それに各種界面活性剤を0.2重量部
添加して塗装作業性を評価した。その結果を表2
に示す。
The present invention relates to a method for forming a selective solar heat absorption coating that can be applied to a solar heat collector and impart selective solar heat absorption properties to the surface thereof, and particularly relates to a high performance selective absorption coating. The present invention provides a method for realizing a membrane. In general, there is a technology to form a selective absorption film as a technology that contributes to improving the efficiency of solar heat collectors.
In this case, attention has been paid to coatings that are excellent in applicability to large areas and are inexpensive. In order to achieve selective absorption with this coating, the combination of its constituent systems is important. Conventional combinations include paints in which fine lead sulfide powder is dispersed in silicone resin, copper copper, manganese dioxide, cobalt oxide, etc., and resins such as acrylic melamine, vinyl, and silicone. Proposed.
The key to improving selective absorption characteristics with paint methods is how to improve emissivity, which tends to be high. In a conventional combination system with a comprehensively balanced configuration, the solar absorption coefficient α is 0.93 to 0.94 and the infrared emissivity ε is 0.4 to 0.5 (when the base material is stainless steel). The standard was that it had selective absorption. This level is a high level of emissivity compared to selective absorption films other than paint. If you want to improve the emissivity of a conventional composition system, you just need to make the film thinner, but it is very difficult to apply a thin, stable and uniform coating, and if you make the film thinner, , the number of defects such as pinholes increases, the physical properties of the coating film deteriorate, and the solar absorption rate also decreases. In view of the above-mentioned conventional drawbacks, the present invention aims to prevent defects such as pinholes in the coating film as much as possible.
The object of the present invention is to provide a method that improves painting workability and achieves excellent selective absorption. In order to achieve the above object, the present invention combines a carboxylic acid amide copolymer with Fe, Mn, Cu, Cr, Co,
Using a solvent-based paint whose main components are an oxide or composite oxide containing one or more elements selected from the group of Ni and a low molecular weight tetrafluoroethylene resin, the solid content in the paint is adjusted to the weight fraction. As less than 10wt%,
With amino-modified silicone resin added,
It is applied onto a heat collecting surface and then heated and cured. The above-mentioned carboxylic acid amide copolymer is a binder and is used to form a film on a heat-collecting surface material such as metal. That is, it is for adhering to the substrate and for adhering other coating film components to each other. In addition, oxides or composite oxides containing one or more elements selected from the group of Fe, Mn, Cu, Cr, Co, and Ni are black pigments that absorb sunlight and have low absorption of infrared rays. It is used as Regarding absorption of infrared rays, it is inevitable that all resins absorb a considerable amount of infrared rays, but carboxylic acid amide copolymer is a resin that absorbs relatively little infrared rays. Furthermore, the low molecular weight tetrafluoroethylene resin is used to improve the physical properties of the coating film, and by employing this resin, corrosion resistance, abrasion resistance, impact resistance, heat resistance, etc. are improved. In addition, this low molecular weight 4
Fluorinated ethylene resin contributes. Furthermore, in order to lower the emissivity of the heat collecting surface, a material with a low surface emissivity is used and utilized. Furthermore, in order not to impair the low emissivity of the material, it is desirable that the coating film to be formed be as thin as possible. In order to form a stable and uniform thin coating, it is best to apply the coating with a small amount of solids in the coating. In other words, this is why the solid content in the paint is set to 10wt% or less in terms of weight fraction.For example, if the solid content is expressed as awt% in weight fraction, the dilution of the paint is approximately 100/a. If the dilution is 5 wt%, the dilution is approximately 20 times, and it is calculated that a dry film thickness of 1 μm is obtained with a wet film thickness of 20 μm. By doing so, it becomes possible to form a stable thin film. In conventional paints, under such a highly diluted state, the pigment and resin separate, which tends to cause various paint film defects such as pinholes, but in the case of the present invention, amino-modified Since it contains silicone resin and maintains a stable surface tension state, there is no concern about the occurrence of paint film defects and stable painting operations are possible. After coating in this manner, a selective absorption coating film with excellent performance can be easily formed by heating and curing in an ordinary baking oven. The carboxylic acid amide copolymer in the present invention is
Preferably, a copolymer containing acrylamide, an α,β monoethylenically unsaturated carboxylic acid such as methacrylamide, an acrylic acid alkyl ester, or the like as a main component is preferably used. This is because these resins have excellent properties in terms of weather resistance, heat resistance, corrosion resistance, hardness, thin coating properties, and the like. Pigments include Fe 3 O 4 , MnO 2 , CuO, Co 3 O 4 , NiO selected from the group of Fe, Mn, Cu, Cr, Co, Ni, etc. alone or in mixtures, especially Fe 2 O 3 −
A mixture such as MnO 2 ·CuO or CuO-Cr 2 O 3 is particularly good in terms of transparency in the infrared region and absorption in the sunlight absorption region. Also, for these pigments, the particle size is a particularly important factor, with 0.01
A particle size range of ~0.5 μm is desirable from the standpoint of selective absorption, particularly light scattering. Hereinafter, effects will be explained focusing on examples of the present invention. In addition, evaluation of selective absorption was performed by the following method. Evaluation of absorption rate α is made by Shimadzu Corporation.
Using an MPS-5000 type self-recording spectrophotometer (incident angle 8 degrees, with an integrating sphere reflector), the emissivity of a black body of 6000 was calculated from the measured values at wavelengths between 0.3 and 2.0 μm. . In addition, the evaluation of emissivity (ε) is
DEVICES & SERVICES COMPANY D
Direct evaluation was performed using an andS AERD type emissivity meter. Example: The test piece is 70mm x 150mm x 0.3mm.
Stainless steel YUS− made by Nippon Steel Corporation with dimensions of
190 (trade name) was used, and the paint was prepared according to the formulation shown in Table 1. This paint has a solids content of approximately 34%. When this paint is diluted with a solvent of the same composition as the paint in order to apply a thin film with a thickness of approximately 1 μm,
It is possible to dilute an area of at most 15% without causing unevenness (pinholes, flutters) on the coated surface.
If this is applied simply by spray painting, it is possible to increase the dilution, but it is difficult to do so by electrostatic painting using a disk. Therefore, coating workability was evaluated by adding 0.2 parts by weight of various surfactants to 15 parts by weight of the paint shown in Table 1 and 85 parts by weight of the solvent. Table 2 shows the results.
Shown below.
【表】【table】
【表】
表2からも明らかなように、アミノ変性シリコ
ーンを添加した場合に、塗装作業性の改善に関し
て効果が見られた。
塗料調合の段階で加えておいた場合でも同様の
効果が得られることを確認した。これらの添加剤
は表面張力を変化させ、溶剤蒸発に伴う移動現象
に関して、顔料〜樹脂系の分離をなんらかの形で
抑制しているものと考えられる。
なお、これらの添加剤の添加量は、0.05wt%か
ら有効であつた。そして添加量が1wt%となる
と、塗膜物性に悪影響、すなわち塗膜の耐蒸気性
等を劣化させる傾向が表われる。
このような組み合わせ系により、始めて約1μ
mの膜厚レベルでの安定した選択吸収塗膜形成が
可能となる。
図面は本発明の方法により、ステンレス
(YUS−190)板上に形成した塗膜の膜厚と選択
吸収性(α、ε)との関係を示したもので、例え
ば、0.8μmの膜厚の場合、αが0.92、εが0.26と
極めて優れた選択吸収性が得られている。
以上のように本発明の方法は、既存の塗装設備
を用いて、工業的に量産が簡単に行なえるもので
あり、その実用的効果は極めて大きいものであ
る。[Table] As is clear from Table 2, the addition of amino-modified silicone was effective in improving painting workability. It was confirmed that similar effects can be obtained even when added at the paint formulation stage. It is believed that these additives change the surface tension and somehow suppress the separation of the pigment and resin system with respect to the migration phenomenon accompanying solvent evaporation. Note that the amount of these additives added was effective from 0.05 wt%. When the amount added is 1 wt%, there is a tendency to have an adverse effect on the physical properties of the coating film, that is, to deteriorate the vapor resistance of the coating film. With such a combination system, for the first time approximately 1μ
It becomes possible to form a stable selective absorption coating film at a film thickness level of m. The drawing shows the relationship between the film thickness and selective absorption properties (α, ε) of a coating film formed on a stainless steel (YUS-190) plate by the method of the present invention. In this case, extremely excellent selective absorption was obtained with α of 0.92 and ε of 0.26. As described above, the method of the present invention can be easily mass-produced industrially using existing coating equipment, and its practical effects are extremely large.
図は本発明の方法により形成した選択吸収塗膜
の膜厚と選択吸収性との関係を示すグラフであ
る。
The figure is a graph showing the relationship between the film thickness and selective absorption property of the selective absorption coating film formed by the method of the present invention.
Claims (1)
Cu、Cr、Co、Niの群から選択した1種以上の元
素を含む酸化物または複合酸化物と、低分子量4
フツ化エチレン樹脂を主成分とする溶剤系塗料を
用いて、塗料中の固形分率を重量分率で10wt%
以下として、アミノ変性シリコーン樹脂を添加し
た状態にて、集熱面上に塗布し、その後、加熱硬
化させるようにした太陽熱選択吸収塗膜の形成方
法。1 Carboxylic acid amide copolymer, Fe, Mn,
An oxide or composite oxide containing one or more elements selected from the group of Cu, Cr, Co, and Ni, and a low molecular weight 4
Using a solvent-based paint whose main component is fluorinated ethylene resin, the solid content in the paint is reduced to 10wt% by weight.
The following is a method for forming a solar heat selective absorption coating film, which is coated on a heat collecting surface in a state in which an amino-modified silicone resin is added, and then heated and cured.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57078927A JPS58195746A (en) | 1982-05-10 | 1982-05-10 | Method of forming solar heat selective absorption coating film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57078927A JPS58195746A (en) | 1982-05-10 | 1982-05-10 | Method of forming solar heat selective absorption coating film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58195746A JPS58195746A (en) | 1983-11-15 |
| JPS6337862B2 true JPS6337862B2 (en) | 1988-07-27 |
Family
ID=13675497
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57078927A Granted JPS58195746A (en) | 1982-05-10 | 1982-05-10 | Method of forming solar heat selective absorption coating film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58195746A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2566122C1 (en) | 2011-11-22 | 2015-10-20 | Ниппон Стил Энд Сумитомо Метал Корпорейшн | Heat-resistant ferritic steel and method of its manufacturing |
-
1982
- 1982-05-10 JP JP57078927A patent/JPS58195746A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58195746A (en) | 1983-11-15 |
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