JPS623184B2 - - Google Patents
Info
- Publication number
- JPS623184B2 JPS623184B2 JP56105790A JP10579081A JPS623184B2 JP S623184 B2 JPS623184 B2 JP S623184B2 JP 56105790 A JP56105790 A JP 56105790A JP 10579081 A JP10579081 A JP 10579081A JP S623184 B2 JPS623184 B2 JP S623184B2
- Authority
- JP
- Japan
- Prior art keywords
- absorption
- solar heat
- manganese
- emissivity
- paint
- 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
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 16
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- 239000003973 paint Substances 0.000 claims description 11
- 239000011347 resin Substances 0.000 claims description 11
- 229920005989 resin Polymers 0.000 claims description 11
- 239000000049 pigment Substances 0.000 claims description 9
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 8
- 229910052802 copper Inorganic materials 0.000 claims description 8
- 239000010949 copper Substances 0.000 claims description 8
- 150000002484 inorganic compounds Chemical class 0.000 claims description 8
- 229910010272 inorganic material Inorganic materials 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 8
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 7
- 229910052804 chromium Inorganic materials 0.000 claims description 7
- 239000011651 chromium Substances 0.000 claims description 7
- 239000010941 cobalt Substances 0.000 claims description 7
- 229910017052 cobalt Inorganic materials 0.000 claims description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 7
- 239000002131 composite material Substances 0.000 claims description 7
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 239000002245 particle Substances 0.000 claims description 7
- 239000008199 coating composition Substances 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 5
- 239000004925 Acrylic resin Substances 0.000 claims description 4
- 229920000178 Acrylic resin Polymers 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 2
- 229920002050 silicone resin Polymers 0.000 claims description 2
- 238000010521 absorption reaction Methods 0.000 description 22
- 238000000576 coating method Methods 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 description 2
- 230000031700 light absorption Effects 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- MIVBAHRSNUNMPP-UHFFFAOYSA-N manganese(2+);dinitrate Chemical compound [Mn+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O MIVBAHRSNUNMPP-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910001960 metal nitrate Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 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
- F24S70/225—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)
- 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)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
本発明は、太陽熱の集熱器表面に適用され、主
として金属の集熱器表面に塗装することにより、
その表面に太陽熱の選択吸収性を持たせるための
塗料組成物に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention is applied to the surface of a solar heat collector, mainly by coating the surface of a metal heat collector.
The present invention relates to a coating composition for imparting selective absorption of solar heat to its surface.
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、既に給湯などを目的
として実用化が進んでいる。 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.
太陽熱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、その吸収された太陽エネル
ギーにより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。 Desirable characteristics for the surface of a solar collector that collects solar thermal energy are those that absorb as much solar energy as possible and minimize the amount of radiant energy that is dissipated from the surface whose temperature has increased due to the absorbed solar energy (selection). absorbency).
一般に大気圏を通過して来た太陽光線の放射エ
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80〜1000℃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。出入この波長のずれを利用して、
2.5μm以下では、その吸収率が1に近いほど、
理想的な選択吸収面となる。 In general, most of the radiant energy of sunlight that passes through the atmosphere is on the short wavelength side of 0.2 to 2.5 μm, and on the other hand, that energy is absorbed as heat and released from surfaces heated to 80 to 1000 degrees Celsius. The radiant energy dissipated is in the infrared region with long wavelengths of 2.5 μm or more. Taking advantage of this wavelength shift,
Below 2.5 μm, the closer the absorption rate is to 1, the more
It becomes an ideal selective absorption surface.
また塗料を用いて、金属面上に塗膜を形成して
太陽熱の選択吸収面とするためには、2.5μm以
下の波長の光の吸収性に優れている黒色顔料を用
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、2.5μm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、如何にして、放射率を低くするかが課題
となる。 In addition, in order to form a coating film on a metal surface using paint to make it a surface that selectively absorbs solar heat, it is possible to use a black pigment that has excellent absorption of light with a wavelength of 2.5 μm or less. Although the absorption rate can be increased relatively easily, since a typical coating film also absorbs light with a wavelength of 2.5 μm or more, the emissivity of light with a wavelength of 2.5 μm or more also increases. Therefore, the problem is how to lower the emissivity.
これを達成するための一般的な考え方として
は、金属表面は赤外線を良く反射するため、極
力、塗膜の膜厚を数μm以下と薄くして、2.5μ
m以上の赤外線の吸収を少なく、すなわち放射率
を低くとどめる方法がある。 The general idea to achieve this is to make the coating film as thin as possible, to a few μm or less, since metal surfaces reflect infrared rays well.
There is a method to reduce the absorption of infrared rays of m or more, that is, to keep the emissivity low.
この方法の場合、塗料成分をある程度選択する
ことにより、選択吸収性を発揮させることができ
るが、塗膜の金属との密着性が悪い、あるいは、
薄い膜厚の塗膜を工業的に安定して塗装すること
が極めて困難であるなどの背景から、未だ実用化
に至つていない。 In this method, selective absorption can be achieved by selecting the paint components to a certain extent, but the adhesion of the paint film to the metal is poor, or
It has not yet been put to practical use because it is extremely difficult to apply a thin coating film in an industrially stable manner.
本発明は、選択吸収性と塗膜物性とをバランス
良く両立させるとともに、塗装作業性においても
優れている太陽熱の選択吸収用塗料組成物を提供
するものである。 The present invention provides a coating composition for selectively absorbing solar heat that achieves both selective absorption and physical properties of the coating film in a well-balanced manner and is also excellent in coating workability.
本発明の塗料組成物を適用すべき被塗装面とし
ては、放射率の低い金属面が有利であり、銅、ア
ルミニウム、ステンレスなどが挙げられる。 The surface to be coated to which the coating composition of the present invention is applied is advantageously a metal surface with a low emissivity, such as copper, aluminum, stainless steel, etc.
本発明の塗料は、粒径が0.2μm以下の無機化
合物微粉末上に、鉄、マンガン、銅、ニツケル、
クロム、コバルトの群から選んだ1種以上の酸化
物または複合酸化物を担持した顔料と透明性樹脂
を溶剤とともに混合し、かつボールミル、アトラ
イタなどの分散機で分散させることにより得られ
る。なお、この塗料には必要に応じて、界面活性
剤などの補助剤や充填剤なども配合して用いるこ
とが可能であり、また透明性樹脂の10%程度、改
質のための樹脂も添加できる。 The paint of the present invention is made of iron, manganese, copper, nickel,
It can be obtained by mixing a pigment supporting one or more oxides or composite oxides selected from the group of chromium and cobalt and a transparent resin with a solvent, and then dispersing the mixture using a dispersing machine such as a ball mill or an attritor. Furthermore, if necessary, auxiliary agents such as surfactants and fillers can be added to this paint, and about 10% of the transparent resin can also be added to modify the resin. can.
既に述べたように本発明の塗料に要求される性
質としては、極力薄い膜厚でも、太陽光の吸収率
が高いこと、また2.5μm以上の赤外線にはでき
るだけ透明であることが挙げられる。バインダー
が有機性樹脂である以上、分子の回転、振動に伴
う赤外線の吸収は避けられない。バインダーとし
て塗料に用いることが可能な有機性樹脂の中で、
透明性樹脂として、太陽熱吸収用の塗料におい
て、適用可能な樹脂は、アクリル樹脂、シリコー
ン樹脂、フツ素樹脂が挙げられる。太陽熱集熱器
としての用途に関係して要求される耐熱性に応じ
て樹脂は使に分けられるが、家庭用の給湯用で
は、アクリル樹脂で十分であると考えられる。 As already mentioned, the properties required of the paint of the present invention include high absorption of sunlight even at the thinnest film thickness, and transparency as much as possible to infrared rays of 2.5 μm or more. Since the binder is an organic resin, absorption of infrared rays due to molecular rotation and vibration is unavoidable. Among the organic resins that can be used as binders in paints,
Examples of transparent resins that can be used in coatings for solar heat absorption include acrylic resins, silicone resins, and fluorine resins. Resins are classified into different types depending on the heat resistance required for use as a solar heat collector, but acrylic resins are considered to be sufficient for domestic hot water supply.
また選択吸収性に好ましい顔料としては、鉄、
マンガン、銅、ニツケル、クロム、コバルトの群
から選択した1種以上の酸化物または複合酸化物
が挙げられる。これは、赤外線の吸収も余りな
く、かつ太陽光の吸収が良好であるためである
が、膜厚と吸収率、放射率との間に関係があり、
膜厚が厚くなると吸収率、放射率ともに高くな
り、膜厚が薄くなると吸収率、放射率とも低くな
る。したがつて、最適の膜厚があることになる。
この種の無機顔料を使用している限りは、性能に
限界があり、吸収率αが0.93〜0.94、放射率εが
0.35〜0.45(基材により幅がある)がその限界で
あつた。 In addition, preferable pigments for selective absorption include iron,
Examples include one or more oxides or composite oxides selected from the group of manganese, copper, nickel, chromium, and cobalt. This is because there is little absorption of infrared rays and good absorption of sunlight, but there is a relationship between film thickness, absorption rate, and emissivity.
As the film thickness increases, both absorption rate and emissivity increase, and as the film thickness decreases, both absorption rate and emissivity decrease. Therefore, there is an optimum film thickness.
As long as this type of inorganic pigment is used, there are limits to its performance, with an absorption rate α of 0.93 to 0.94 and an emissivity ε.
The limit was 0.35 to 0.45 (the range varies depending on the base material).
本発明は、低い膜厚でも吸収率を高めようとの
観点から、その効果に関して中心的な役割を果し
ている顔料に注目したものである。 The present invention focuses on pigments, which play a central role in this effect, from the viewpoint of increasing the absorption rate even with a low film thickness.
次に本発明で用いる顔料の製法について詳述す
る。シリカ、アルミナ、二酸化チタン、タルク、
カオリン、炭酸カルシウム等の無機化合物の微粒
子を用いる。これらの無機化合物を担体として、
この担持上に、鉄、マンガン、銅、ニツケル、ク
ロム、コバルトの群から選んだ1種以上の酸化物
または複合酸化物を担持させる。その方法は、
鉄、マンガン、銅、ニツケル、クロム、コバルト
の硝酸塩水溶液中に、前述した無機化合物を浸漬
して、含浸乾燥させる。このような操作の後、こ
れをアンモニア水中に入れる。これにより、金属
の硝酸塩は水酸化物となる。これを水洗し、乾燥
した後、約500℃で空気中で焼成する。このよう
にして、無機化合物上に、鉄、マンガン、銅、ニ
ツケル、クロム、コバルトの群から選んだ1種以
上の酸化物または複合酸化物を担持した顔料が調
整される。 Next, the method for producing the pigment used in the present invention will be described in detail. Silica, alumina, titanium dioxide, talc,
Fine particles of inorganic compounds such as kaolin and calcium carbonate are used. Using these inorganic compounds as a carrier,
On this support, one or more oxides or composite oxides selected from the group of iron, manganese, copper, nickel, chromium, and cobalt are supported. The method is
The above-mentioned inorganic compound is immersed in an aqueous solution of nitrates of iron, manganese, copper, nickel, chromium, and cobalt, and is impregnated and dried. After such manipulation, it is placed in ammonia water. As a result, the metal nitrate becomes a hydroxide. After washing with water and drying, it is fired in air at approximately 500°C. In this way, a pigment is prepared in which one or more oxides or composite oxides selected from the group of iron, manganese, copper, nickel, chromium, and cobalt are supported on an inorganic compound.
以下に実施例を中心としてその効果を述べる。 The effects will be described below, focusing on examples.
実施例
無機化合物微粒子として、γ−アルミナの微粉
末を用いた。これを分級して、0.2μ〜0.5μ、0.1
〜0.2μm、0.1μm以下の3種類に分けた。これ
を100℃で1時間乾燥した後、1N−硝酸マンガ
ン、1N−硝酸第2鉄を含む水溶液中に一昼夜浸
漬した後、100℃で2時間乾燥した。これをブロ
ナーロート上に移し、そして2N−アンモニア水
で洗浄した後、アンモニアの痕跡がなくなるまで
水洗し、さらに100℃で1時間乾燥した後、500℃
で2時間焼成した。このようにして調整した顔料
25重量部に、アクリル樹脂としての三菱レーヨン
(株)製の「ダイヤナールSE−5661」を100重量部、
溶剤としてのソルベツソ#100を100重量部、n−
ブタノールを58重量部、キシレンを42重量部加え
て混合し、そしてアトライタを用いて、6時間分
散させて塗料化した。このようにして調整した塗
料を溶剤により2.5倍に希釈して、純アルミニウ
ム板上に1μmの膜厚にて塗装し、その吸収率
α、放射率εを評価した。この結果、0.2μ〜0.5
μの初期粒径の場合、α=0.85、ε=0.35、0.1〜
0.2μmの粒径の場合、α=0.95、ε=0.25、0.1
μm以下の粒径の場合、α=0.95、ε=0.24の結
果を得た。Example Fine powder of γ-alumina was used as the inorganic compound fine particles. Classify this to 0.2μ ~ 0.5μ, 0.1
It was divided into three types: ~0.2 μm and 0.1 μm or less. After drying this at 100°C for 1 hour, it was immersed in an aqueous solution containing 1N manganese nitrate and 1N ferric nitrate all day and night, and then dried at 100°C for 2 hours. This was transferred onto a Bronner funnel, washed with 2N ammonia water, washed with water until there was no trace of ammonia, dried at 100°C for 1 hour, and then heated to 500°C.
It was baked for 2 hours. Pigments prepared in this way
25 parts by weight, Mitsubishi Rayon as acrylic resin
100 parts by weight of “Dianal SE-5661” manufactured by Co., Ltd.
100 parts by weight of Solbetuso #100 as a solvent, n-
58 parts by weight of butanol and 42 parts by weight of xylene were added and mixed, and dispersed for 6 hours using an attritor to form a paint. The paint prepared in this way was diluted 2.5 times with a solvent and painted on a pure aluminum plate to a film thickness of 1 μm, and its absorption rate α and emissivity ε were evaluated. As a result, 0.2μ ~ 0.5
For initial particle size of μ, α=0.85, ε=0.35, 0.1~
For particle size of 0.2μm, α=0.95, ε=0.25, 0.1
In the case of particle sizes of μm or less, results of α=0.95 and ε=0.24 were obtained.
0.2μm以下の粒径の場合に、α=0.95と高い
吸収率が得られたのは、無機化合物粒子を含む中
心核として、その表面に安定な鉄、マンガンの複
合酸化物が形成され、それが光の吸収に対して、
干渉膜的な効果を発揮して、吸収率を向上させた
ものと考えられる。 The reason why a high absorption rate of α=0.95 was obtained when the particle size was 0.2 μm or less was due to the formation of a stable composite oxide of iron and manganese on the surface of the central core containing the inorganic compound particles. is for light absorption,
It is thought that it exerts an effect like an interference film and improves the absorption rate.
このような表面構造にした場合、塗料化のため
の分散操作の際に破壊されてしまうのではないか
と懸念されたが、そのような影響は現実にはなか
つた。 There was a concern that such a surface structure would be destroyed during the dispersion operation for making it into a paint, but such an effect did not actually occur.
以上のように本発明の塗料組成物は、粒径が
0.2μm以下の無機化合物微粉末上に、鉄、マン
ガン、銅、ニツケル、クロム、コバルトの群から
選んだ1種以上の酸化物または複合酸化物を担持
した顔料と透明性樹脂を溶剤とともに混合してい
るため、この塗料組成物を放射率の小さな金属面
上に塗装して焼き付けることにより、極めて経済
的で、かつ安価にして、優れた太陽熱の選択吸収
面を得ることができる。 As described above, the coating composition of the present invention has a particle size of
A pigment supporting one or more oxides or composite oxides selected from the group of iron, manganese, copper, nickel, chromium, and cobalt and a transparent resin are mixed with a solvent on inorganic compound fine powder of 0.2 μm or less. Therefore, by coating and baking this coating composition on a metal surface with a low emissivity, it is possible to obtain an excellent selective absorption surface of solar heat at a very economical and low cost.
Claims (1)
に、鉄、マンガン、銅、ニツケル、クロム、コバ
ルトの群から選んだ1種以上の酸化物または複合
酸化物を担持した顔料と透明性樹脂を溶剤ととも
に混合してなる太陽熱の選択吸収用塗料組成物。 2 前記透明性樹脂として、アクリル樹脂、シリ
コーン樹脂、フツ素樹脂の群から選んだ1種以上
を用いてなる特許請求の範囲第1項記載の太陽熱
の選択吸収用塗料組成物。[Claims] 1. One or more oxides or composite oxides selected from the group of iron, manganese, copper, nickel, chromium, and cobalt are supported on inorganic compound fine powder with a particle size of 0.2 μm or less. A paint composition for selectively absorbing solar heat, which is made by mixing a pigment and a transparent resin with a solvent. 2. The coating composition for selectively absorbing solar heat according to claim 1, wherein the transparent resin is one or more selected from the group of acrylic resins, silicone resins, and fluororesins.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56105790A JPS587460A (en) | 1981-07-06 | 1981-07-06 | Coating composition for selective absorption of solar heat |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP56105790A JPS587460A (en) | 1981-07-06 | 1981-07-06 | Coating composition for selective absorption of solar heat |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS587460A JPS587460A (en) | 1983-01-17 |
| JPS623184B2 true JPS623184B2 (en) | 1987-01-23 |
Family
ID=14416922
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP56105790A Granted JPS587460A (en) | 1981-07-06 | 1981-07-06 | Coating composition for selective absorption of solar heat |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS587460A (en) |
-
1981
- 1981-07-06 JP JP56105790A patent/JPS587460A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS587460A (en) | 1983-01-17 |
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