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JPS624625B2 - - Google Patents
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JPS624625B2 - - Google Patents

Info

Publication number
JPS624625B2
JPS624625B2 JP56058907A JP5890781A JPS624625B2 JP S624625 B2 JPS624625 B2 JP S624625B2 JP 56058907 A JP56058907 A JP 56058907A JP 5890781 A JP5890781 A JP 5890781A JP S624625 B2 JPS624625 B2 JP S624625B2
Authority
JP
Japan
Prior art keywords
paint
absorption
solid content
particle size
pigment
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
JP56058907A
Other languages
Japanese (ja)
Other versions
JPS57174647A (en
Inventor
Masao Maki
Ju Fukuda
Seiichi Sano
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 JP56058907A priority Critical patent/JPS57174647A/en
Publication of JPS57174647A publication Critical patent/JPS57174647A/en
Publication of JPS624625B2 publication Critical patent/JPS624625B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/32Radiation-absorbing paints

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Paints Or Removers (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Laminated Bodies (AREA)

Description

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

本発明は、太陽熱を利用した集熱器等における
太陽熱の選択吸収面を製造する方法に関するもの
である。 近年のエネルギー事情から太陽熱利用技術が注
目され、家庭用としても、すでに給湯などを目的
に実用化が進んでいる。 太陽エネルギーを集熱する集熱器の表面に望ま
しい特性としては、太陽エネルギーを極力大量に
吸収するとともに、太陽エネルギーを吸収して温
度上昇した面から放散する放射エネルギーをでき
るだけ少なくする特性(選択吸収性)が挙げられ
る。 大気圏を通過して来た太陽光線の輻射エネルギ
ーは、ほとんどが、0.2〜2.5μmの短波長側にあ
り、一方、そのエネルギーを熱として吸収して、
例えば80〜100℃に加熱された面から放散する放
射エネルギーは、2.5μm以上の長波長の赤外線
域にある。したがつてこの出入りの波長のずれを
利用して、2.5μm以下ではその吸収率が1に近
く、かつ2.5μm以上では、その放射率が0に近
くなるようにすれば、理想的な選択吸収面とな
る。 塗料を用いて、金属面上に塗膜を形成し、この
塗膜を太陽熱の選択吸収面とするためには、2.5
μm以下の波長における光の吸収性が優れた黒色
顔料を用いることによつて、吸収率は比較的容易
に高くすることができるが、通常の塗膜は、2.5
μm以上の光をも吸収してしまうため、2.5μm
以上の波長の光の放射率も同時に高くなつてしま
う。したがつて、いかにして、放射率を低くする
かが課題となる。 塗膜構成要素としては、樹脂,顔料が基本とな
るが、2.5μm以上の光、すなわち赤外線をほと
んどの樹脂は強く吸収してしまうため、放射率を
低くすることは困難である。また顔料に関して
は、無機顔料を用いれば、この無機顔料があまり
赤外線を吸収しないため、放射率の面で非常に有
利である。 そこで、前記樹脂分を相対的に少なくして塗膜
を形成すれば、選択吸収性の面では有利になる
が、金属素地との接着性,顔料相互の接着性は悪
く、したがつて非常に密着性の悪い塗膜となつて
しまう。 また樹脂と顔料との比を、素地の塗膜としての
密着性が保持される範囲とした場合に、放射率を
低くしようとすれば、赤外線の吸収性がなるべく
少なくなるように、樹脂および顔料を選択すると
ともに、塗膜の膜厚をできるだけ薄く形成するこ
とが必要である。この方法の場合には、当然、素
地金属は放射率の少ない金属面であることが前提
となる。 前記放射率の少ない金属としては、アルミニウ
ム,銅,ステンレスなどが最適である。現実に、
これらの金属面に薄い塗膜を形成することを工業
ベースで実施しようとすれば、膜厚管理に伴う困
難が多い。通常の塗料では、着色力,隠蔽力,分
散性,色相などの観点から、1.0μm以上の粒径
の顔料を用いるため、連続した膜を形成しようと
すれば、どうしても10μm以上の膜厚となつてし
まう。この膜厚で、選択吸収能を発揮させること
は、非常に困難である。 またカーボンブラツクは、非常に粒径が細か
く、0.01μmの粒径も可能であるが、顔料として
の赤外線の透明性が悪いため、選択吸収性を得る
ことは困難である。 そしてまた通常の塗料を用いてスプレーにて塗
装する場合には、塗装作業性を良くする観点か
ら、最適の固形分範囲があり、例えば20wt%以
下の固形分の少ない状態で塗装することは少な
い。これは、粘度が低い状態ではだれが発生した
り、顔料が2次凝集を起こしたり、沸きを発生し
たりするためである。 本発明では、無機黒色顔料として、Fe(鉄),
Mn(マンガン),Cu(銅),Cr(クロム),Co
(コバルト),Ni(ニツケル)群から選択した1
種以上の酸化物、複合酸化物を用いる。これら
は、いずれも、ほとんど赤外線の吸収を持たない
ため、良好な太陽光の吸収性を示す。例えば、
CoO・Cr2O3・MnO2・Fe2O3,Fe2O3・MnO・
CuO,CuO,Cr2O3などは優れている。 薄膜形成のための安定した隠蔽力を発揮し、ま
た同時に赤外線の散乱吸収を少なくするために
は、その粒径が重要である。0.01〜0.5μmの粒
径の顔料が最適の特性を示す。 以下、本発明を実施例にもとづいて説明する。 実施例 (1) Fe2O3・MnO・CuO系市販顔料を用いて、その
顔料の粒径を分級し、6種類として試験した。 まず、熱硬化性アクリル樹脂を用いて、樹脂固
形分に対し、52重量%の各顔料を含む塗料を試作
し、この塗料をスプレーにて、ステンレス基板上
に、膜厚が約3μmとなるように塗装し、200℃
にて、10分焼成した。 顔料粒径と選択吸収性との関係を次表に示す。
The present invention relates to a method for manufacturing a selective solar heat absorption surface in a solar heat collector or the like. Due to the energy situation in recent years, solar heat utilization technology has attracted attention, and it is already being put into practical use for household purposes such as hot water heating. Desirable properties for the surface of a heat collector that collects solar energy include the ability to absorb as much solar energy as possible, as well as to minimize the amount of radiant energy radiated from the surface that absorbs solar energy and whose temperature has increased (selective absorption). gender). Most of the radiant energy of sunlight passing through the atmosphere is at the short wavelength side of 0.2 to 2.5 μm, and on the other hand, that energy is absorbed as heat,
For example, the radiant energy radiated from a surface heated to 80 to 100°C is in the infrared region with a long wavelength of 2.5 μm or more. Therefore, by making use of this shift in the wavelengths of ingress and egress, ideal selective absorption can be achieved by making the absorption rate close to 1 below 2.5 μm and the emissivity close to 0 above 2.5 μm. It becomes a surface. In order to form a coating film on a metal surface using paint and make this coating film a surface that selectively absorbs solar heat, 2.5
The absorption rate can be relatively easily increased by using a black pigment that has excellent absorption of light at wavelengths below μm.
2.5 μm because it absorbs light of μm or more.
At the same time, the emissivity of light with wavelengths higher than that also increases. Therefore, the problem is how to lower the emissivity. The basic components of the coating film are resins and pigments, but since most resins strongly absorb light of 2.5 μm or more, that is, infrared rays, it is difficult to lower the emissivity. Regarding pigments, if inorganic pigments are used, this inorganic pigment does not absorb much infrared rays, so it is very advantageous in terms of emissivity. Therefore, if a coating film is formed with a relatively small amount of resin, it will be advantageous in terms of selective absorption, but the adhesion to the metal base and the adhesion between pigments will be poor, and therefore it will be very difficult to form a coating. This will result in a paint film with poor adhesion. In addition, when the ratio of resin and pigment is set within a range that maintains adhesion as a coating film to the base material, if the emissivity is to be lowered, the resin and pigment should be adjusted so that the infrared absorption is as low as possible. It is necessary to select the desired amount and to form the coating film as thinly as possible. In the case of this method, it is naturally assumed that the base metal is a metal surface with low emissivity. As the metal with low emissivity, aluminum, copper, stainless steel, etc. are most suitable. In reality,
If it is attempted to form a thin coating film on these metal surfaces on an industrial basis, there are many difficulties associated with controlling the film thickness. Ordinary paints use pigments with a particle size of 1.0 μm or more from the viewpoint of coloring power, hiding power, dispersibility, hue, etc., so if you want to form a continuous film, you will inevitably end up with a film thickness of 10 μm or more. I end up. It is extremely difficult to exhibit selective absorption ability with this film thickness. Further, carbon black has a very fine particle size, and a particle size of 0.01 μm is possible, but it is difficult to obtain selective absorption properties because of its poor infrared transparency as a pigment. Furthermore, when spray painting with regular paints, there is an optimal solids content range from the perspective of improving painting workability, and it is rare to paint with a low solids content of 20wt% or less, for example. . This is because when the viscosity is low, sagging occurs, secondary aggregation of the pigment occurs, and boiling occurs. In the present invention, Fe (iron),
Mn (manganese), Cu (copper), Cr (chromium), Co
1 selected from the (cobalt), Ni (nickel) group
More than one type of oxide or composite oxide is used. All of these materials have almost no infrared absorption, so they exhibit good sunlight absorption. for example,
CoO・Cr 2 O 3・MnO 2・Fe 2 O 3 , Fe 2 O 3・MnO・
CuO, CuO, Cr 2 O 3 etc. are excellent. The particle size is important in order to exhibit stable hiding power for forming a thin film and at the same time to reduce scattering and absorption of infrared rays. Pigments with a particle size of 0.01-0.5 μm exhibit optimal properties. Hereinafter, the present invention will be explained based on examples. Examples (1) Using commercially available Fe 2 O 3 .MnO.CuO pigments, the particle sizes of the pigments were classified and tested as 6 types. First, we made a prototype paint using thermosetting acrylic resin containing 52% by weight of each pigment based on the solid content of the resin, and sprayed this paint onto a stainless steel substrate to a film thickness of approximately 3 μm. Painted at 200℃
Baked for 10 minutes. The relationship between pigment particle size and selective absorption is shown in the table below.

【表】 上記表からも明らかなように、顔料粒径は、
0.01〜0.5μmの範囲が良好である。これは粒子
の光散乱に関係し、0.01〜0.5μmの範囲が選択
吸収性に関係して、2.0μm以上の長波長側の光
を余り散乱せず、かつ2.0μm以下は良く散乱す
るような性質を示すためと推定される。更に粒径
の細かい側については、反応性が強くなつて2次
凝集を起こしたものかと考えられる。 また太陽熱の選択吸収膜を塗膜にて形成するた
めの樹脂としては、アクリル樹脂,シリコーン樹
脂が比較的赤外域の吸収が少ないことから、望ま
しい。 以下に選択吸収膜(塗膜)の形成方法を述べ
る。 アクリル樹脂またはシリコーン樹脂を用いて、
その樹脂固形分(重量)に対して、50〜60wt%
の重量を有する無機黒色顔料、すなわち、Fe,
Mn,Cu,Cr,Co,Niの群から選択した1種以
上の酸化物、複合酸化物であつて、粒径が0.01〜
0.5μmのものを添加混合して、良く分散させ
る。この分散を良好に行なうために、分散時の固
形分濃度は、25〜50wt%となるように溶剤で稀
釈して行なうのが望ましい。 更にスプレー塗装にて塗装を行なう際には、樹
脂と顔料を合わせた総固形分率(wt%)が、10
〜17wt%となるように溶剤で稀釈して塗装す
る。 これらの樹脂および顔料系を用いて、塗料中の
総固形分率(wt%)を10〜17wt%とした場合
に、塗料の比重はほぼ1となる。また、これらの
乾燥塗膜の比重もほぼ1となるため、乾燥膜厚と
濡れ膜厚との比は、総固形分と塗料総量との比と
一致する。10wt%の場合で10倍、17wt%で約5.9
倍となる。塗料粘度は12.5wt%(すなわち、8倍
付近)でほぼ1ポイズとなる。これは、顔料の粒
径が細かいため、塗料粘度は、通常の粒径(0.5
〜1.5μm)の顔料の場合ほど低下しないためで
ある。 また2〜5μmの乾燥膜厚を得るためには、
10wt%の総固形分率で20〜50μmの濡れ膜厚を
得るように塗装すれば良い。また17wt%では、
約12〜30μmの濡れ膜厚を目標に塗装すれば良
い。 なお、総固形分率を10wt%以下にした場合に
は、濡れ塗膜において、浮きを発生したり、だれ
を起こしたりし易くなり、その扱いが困難となる
ものであり、また他方、17wt%以上とした場合
には、2〜5μmの膜厚を安定して得ることが困
難となるものである。この場合、総固形分率は
12.5〜15wt%の範囲が最良である。 以上のように本発明の方法にて塗膜を形成すれ
ば、下地金属との組み合わせによるが、吸収率α
=0.93〜0.95,放射率ε=0.35〜0.50の塗膜が安
定して得られる。また本発明の方法は、従来より
工業的な生産が行なわれているエアスプレー,静
電塗装等の塗装設備を用いてそのまま塗装できる
ので、極めて実用的となるものである。
[Table] As is clear from the table above, the pigment particle size is
A range of 0.01 to 0.5 μm is good. This is related to the light scattering of particles, and the range of 0.01 to 0.5 μm is related to selective absorption, which means that light with long wavelengths of 2.0 μm or more is not scattered much, and light with wavelengths of 2.0 μm or less is well scattered. It is presumed that this is to show its properties. Furthermore, it is considered that the reactivity of the particles with smaller diameters became stronger and secondary aggregation occurred. Furthermore, as the resin for forming the selective solar heat absorption film as a coating film, acrylic resins and silicone resins are preferable because they have relatively low absorption in the infrared region. The method for forming the selective absorption film (coating film) will be described below. Using acrylic resin or silicone resin,
50 to 60wt% of the resin solid content (weight)
An inorganic black pigment, i.e. Fe, having a weight of
One or more oxides or composite oxides selected from the group of Mn, Cu, Cr, Co, and Ni, with a particle size of 0.01 to
Add and mix 0.5 μm and disperse well. In order to perform this dispersion well, it is desirable to dilute with a solvent so that the solid content concentration during dispersion is 25 to 50 wt%. Furthermore, when painting by spray painting, the total solid content (wt%) of resin and pigment is 10
Dilute with a solvent and paint to a concentration of ~17wt%. When these resins and pigment systems are used and the total solid content (wt%) in the paint is 10 to 17 wt%, the specific gravity of the paint is approximately 1. Further, since the specific gravity of these dry coating films is approximately 1, the ratio of the dry film thickness to the wet film thickness matches the ratio of the total solid content to the total amount of paint. 10 times for 10wt%, about 5.9 for 17wt%
It will be doubled. The paint viscosity is approximately 1 poise at 12.5 wt% (that is, around 8 times as much). This is because the particle size of the pigment is fine, so the paint viscosity is lower than the normal particle size (0.5
This is because it does not decrease as much as in the case of pigments with a diameter of ~1.5 μm). In addition, in order to obtain a dry film thickness of 2 to 5 μm,
The coating may be applied to obtain a wet film thickness of 20 to 50 μm at a total solids content of 10 wt%. Also, at 17wt%,
It is sufficient to aim for a wet film thickness of approximately 12 to 30 μm. Furthermore, if the total solids content is less than 10wt%, the wet coating will tend to float or sag, making it difficult to handle. In the above case, it becomes difficult to stably obtain a film thickness of 2 to 5 μm. In this case, the total solids content is
A range of 12.5-15wt% is best. If a coating film is formed by the method of the present invention as described above, the absorption rate α will depend on the combination with the underlying metal.
= 0.93 to 0.95, and a coating film with emissivity ε = 0.35 to 0.50 can be stably obtained. Furthermore, the method of the present invention is extremely practical because it can be applied directly using painting equipment such as air spray and electrostatic painting that has been conventionally used in industrial production.

Claims (1)

【特許請求の範囲】[Claims] 1 アクリル樹脂,シリコーン樹脂の群から選択
した1種以上の樹脂と鉄,マンガン,銅,クロ
ム,コバルト,ニツケルの群から選択した1種以
上の酸化物,複合酸化物であり、かつ粒径が0.01
〜0.5μmの無機黒色顔料を主たる固型分とした
塗料を用い、この塗料を塗料中の総固形分率が
10wt%〜17wt%の範囲となるよう溶剤で稀釈
し、この稀釈した塗料を被処理金属面に塗布した
後、加熱して2.5μmの塗膜を形成したことを特
徴とする太陽熱の選択吸収面の製造方法。
1 One or more resins selected from the group of acrylic resins and silicone resins and one or more oxides or composite oxides selected from the group of iron, manganese, copper, chromium, cobalt, and nickel, and the particle size is 0.01
A paint whose main solid content is an inorganic black pigment of ~0.5 μm is used, and the total solid content of the paint is
A solar heat selective absorption surface characterized by diluting the paint with a solvent to a range of 10wt% to 17wt%, applying the diluted paint to the metal surface to be treated, and then heating to form a 2.5μm coating film. manufacturing method.
JP56058907A 1981-04-17 1981-04-17 Manufacture of selective absorption surface for solar heat Granted JPS57174647A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56058907A JPS57174647A (en) 1981-04-17 1981-04-17 Manufacture of selective absorption surface for solar heat

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56058907A JPS57174647A (en) 1981-04-17 1981-04-17 Manufacture of selective absorption surface for solar heat

Publications (2)

Publication Number Publication Date
JPS57174647A JPS57174647A (en) 1982-10-27
JPS624625B2 true JPS624625B2 (en) 1987-01-31

Family

ID=13097877

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56058907A Granted JPS57174647A (en) 1981-04-17 1981-04-17 Manufacture of selective absorption surface for solar heat

Country Status (1)

Country Link
JP (1) JPS57174647A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0347883A (en) * 1989-04-26 1991-02-28 Japan Synthetic Rubber Co Ltd Coating composition
GB0203214D0 (en) 2002-02-12 2002-03-27 Rolls Royce Plc A black high temperature emissivity paint

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5818572B2 (en) * 1975-09-29 1983-04-13 ニツポンペイント カブシキガイシヤ Laminate with good photothermal conversion

Also Published As

Publication number Publication date
JPS57174647A (en) 1982-10-27

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