JP2004027241A - Thermal insulation coating and its coating method - Google Patents

Thermal insulation coating and its coating method Download PDF

Info

Publication number
JP2004027241A
JP2004027241A JP2003354259A JP2003354259A JP2004027241A JP 2004027241 A JP2004027241 A JP 2004027241A JP 2003354259 A JP2003354259 A JP 2003354259A JP 2003354259 A JP2003354259 A JP 2003354259A JP 2004027241 A JP2004027241 A JP 2004027241A
Authority
JP
Japan
Prior art keywords
pigment
heat
shielding paint
resin
coating
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.)
Pending
Application number
JP2003354259A
Other languages
Japanese (ja)
Inventor
Keigo Kinoshita
木下 啓吾
Noriyasu Noda
野田 憲康
Noriyuki Fukae
深江 典之
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.)
HOUSE TEC KK
NAGASHIMA TOKUSHU TORYO KK
Original Assignee
HOUSE TEC KK
NAGASHIMA TOKUSHU TORYO KK
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 HOUSE TEC KK, NAGASHIMA TOKUSHU TORYO KK filed Critical HOUSE TEC KK
Priority to JP2003354259A priority Critical patent/JP2004027241A/en
Publication of JP2004027241A publication Critical patent/JP2004027241A/en
Pending legal-status Critical Current

Links

Images

Landscapes

  • Paints Or Removers (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a thermal insulation coating having excellent reflecting properties in a near-infrared range even if the coating is black or dark chromatic color near black, capable of preventing a coated film from temperature rise and having excellent weather resistance. <P>SOLUTION: This thermal insulation coating comprises a vehicle of excellent weather resistance and a pigment having 15% or more of reflectance of solar radiation defined by JIS A 5759 and 24 or less of L* value in a color space of L*, a* and b* of CIE 1976. <P>COPYRIGHT: (C)2004,JPO

Description

 本発明は、太陽熱等に対して遮蔽効果を有する遮熱性塗料及びその塗装方法に関する。さらに詳しくは、濃彩色の塗料であっても熱としての吸収が少なく、そのため優れた耐候性を発揮する遮熱性塗料及びその塗装方法に関する。 The present invention relates to a heat-shielding paint having a shielding effect against solar heat and the like, and a coating method thereof. More specifically, the present invention relates to a heat-shielding paint that exhibits low weather absorption even for a dark-colored paint and therefore exhibits excellent weather resistance, and a method of applying the same.

 省エネルギー等の観点から、太陽熱等に対して遮蔽効果を有する遮熱性塗料について、従来数多くの提案がなされている。しかし、それらの多くが白色又はそれに近い淡彩色に限ったものであり、黒色又はそれに近い濃彩色についてのものではない。濃彩色の塗料には通常、カーボンブラックや鉄黒等の顔料が使用されるが、これらは淡彩色に比較すると、紫外から近赤外領域にわたる広い波長域で太陽光を吸収しやすく、そのため塗膜を通じて屋内等の温度上昇を招く。さらに、塗膜中の樹脂が熱劣化することによって、塗膜の白亜化、変退色等を引き起こす。これらの現象は特に、濃彩色でかつ艶消しの塗膜においてより顕著に見られる。 From the viewpoint of energy saving, etc., many proposals have been made on heat-shielding paints having a shielding effect against solar heat or the like. However, most of them are limited to white or near light colors, and not to black or near dark colors. Pigments such as carbon black and iron black are usually used for dark-colored paints.However, compared to light-colored paints, these pigments easily absorb sunlight in a wide wavelength range from the ultraviolet to the near infrared. The temperature rises indoors through the membrane. Further, thermal degradation of the resin in the coating film causes chalking, discoloration and the like of the coating film. These phenomena are particularly pronounced in dark and matte coatings.

 黒色又は濃彩色の遮熱性塗料に関する従来技術として、紫外及び近赤外領域で高い反射率を示す赤、橙、黄、緑、青、紫系顔料のいずれか2種以上を、加法混色することによりマンセル記号N−1の黒とする技術が(特許文献1)で開示されている。この技術により、近赤外領域において吸収を示さない塗膜が得られ温度上昇を抑えることができるが、一方で加法混色した各顔料の耐候性が異なるため、使用中に耐候性の弱い顔料が変退色することによって塗膜全体の色合いが本来の黒色から紫、緑、オレンジ色等に変色するという問題点がある。また、加法混色によってマンセル記号N−1の黒を調整することは極めて難しい。 As a conventional technique relating to black or dark colored heat-shielding paints, two or more of red, orange, yellow, green, blue, and violet pigments exhibiting high reflectance in the ultraviolet and near-infrared regions are additively mixed. (Patent Literature 1) discloses a technique for making the Munsell symbol N-1 black. With this technology, a coating film that does not show absorption in the near-infrared region can be obtained and the temperature rise can be suppressed.On the other hand, since the weather resistance of each additive color-mixed pigment is different, a pigment with weak weather resistance during use can be used. There is a problem that the color of the entire coating film changes from the original black color to purple, green, orange, or the like due to discoloration. Further, it is extremely difficult to adjust black of the Munsell symbol N-1 by additive color mixture.

特開平4−255769号公報JP-A-4-255768

 以上述べたように、従来の黒色又は濃彩色の遮熱性塗料は、耐候性、保色性等の点で不十分であり、また塗料の色相調整も困難であった。そこで本発明は、黒色又は濃彩色の塗料であっても、近赤外領域の反射特性に優れ、そのため塗膜の温度上昇を防ぐことができて耐候性に優れる新規遮熱性塗料を提供するものである。さらに遮熱性塗料の耐候性をより効果的に発揮させることができる塗装方法を提供するものである。 As described above, the conventional heat-shielding paint of black or dark color was insufficient in terms of weather resistance and color retention, and it was difficult to adjust the hue of the paint. Therefore, the present invention provides a novel heat-shielding paint having excellent reflection characteristics in the near-infrared region even if it is a black or dark-colored paint, thereby preventing a rise in temperature of the coating film and having excellent weather resistance. It is. It is another object of the present invention to provide a coating method capable of more effectively exhibiting the weather resistance of the heat-shielding paint.

 上記課題を解決するため、本発明は、可視領域で吸収を示し近赤外領域では反射を示す顔料と、耐候性に優れるビヒクルとを含有する塗料としたことを特徴とする。 た め In order to solve the above problems, the present invention is characterized in that a paint containing a pigment that absorbs in the visible region and reflects in the near infrared region and a vehicle having excellent weather resistance are provided.

 また本発明は、前記顔料が、JIS A 5759に定義される日射反射率が15%以上であって、かつCIE1976L* a* b* 色空間におけるL* 値が24以下の顔料であることを特徴とする。 Further, the present invention is characterized in that the pigment has a solar reflectance of 15% or more as defined in JIS A # 5759 and an L * value of 24 or less in a CIE1976 L * a * b * color space. And

 さらに本発明は、前記顔料の含有量が、塗料の樹脂固形分100重量部に対して7〜110重量部であることを特徴とする。 {Further, the present invention is characterized in that the content of the pigment is 7 to 110 parts by weight based on 100 parts by weight of the resin solid content of the paint.

 さらに本発明は、前記顔料に加えて、JIS A 5759に定義される日射反射率が12%以上である着色顔料を少なくとも一種以上と、白色顔料とを含有することを特徴とする。 {Furthermore, the present invention is characterized in that, in addition to the pigment, at least one or more color pigments having a solar reflectance of 12% or more defined in JIS A 5759 and a white pigment.

 前記の、可視領域で吸収を示し近赤外領域では反射を示す顔料と、着色顔料、及び白色顔料の含有量は、塗料の樹脂固形分100重量部に対してそれぞれ7〜110重量部、7〜100重量部、及び40〜230重量部であることが好ましい。 The pigment, which absorbs in the visible region and reflects in the near-infrared region, the content of the color pigment, and the content of the white pigment are 7 to 110 parts by weight, It is preferably from 100 to 100 parts by weight and from 40 to 230 parts by weight.

 また前記白色顔料としては、酸化チタン顔料が好適に用いられる。 チ タ ン A titanium oxide pigment is preferably used as the white pigment.

 さらに本発明の遮熱性塗料は、含有する顔料の平均粒子径が50μm以下に分散されていることを特徴とする。 Furthermore, the heat-shielding paint of the present invention is characterized in that the pigment contained therein has an average particle diameter of 50 μm or less.

 さらに本発明は、セラミックバルーン及び構造保持剤を含有することを特徴とする。これによって高い反射性能が得られると共に、断熱性、防水性等の機能を付与することができる。 Furthermore, the present invention is characterized by containing a ceramic balloon and a structure retaining agent. Thereby, high reflection performance can be obtained, and functions such as heat insulation and waterproofness can be provided.

 また本発明に用いる耐候性に優れるビヒクルは、アクリル樹脂、ポリエステル樹脂、シリコン変性ポリエステル樹脂、シリコン変性アクリル樹脂、アルキッド樹脂、塩化ビニル樹脂、及びフッ素系樹脂の少なくとも一種以上と、必要に応じ、イソシアネート、メラミン樹脂の少なくとも一種以上とを含有することを特徴とする。 The vehicle having excellent weather resistance used in the present invention includes at least one of an acrylic resin, a polyester resin, a silicon-modified polyester resin, a silicon-modified acrylic resin, an alkyd resin, a vinyl chloride resin, and a fluororesin, and if necessary, an isocyanate. And at least one melamine resin.

 さらに本発明は、上述の遮熱性塗料を、塗膜厚が8μm以上になるように塗装し、必要に応じて、下塗り及び/又は上塗りを施すことを特徴とする遮熱性塗料の塗装方法である。下塗り及び/又は上塗りを施すことにより、塗膜全体としての耐久性、耐候性、耐汚染性等をより高めることができる。 Further, the present invention is a method for applying a heat-shielding paint, which comprises applying the above-mentioned heat-shielding paint so that the coating thickness becomes 8 μm or more, and applying an undercoat and / or an overcoat as required. . By applying the undercoat and / or the overcoat, the durability, weather resistance, stain resistance and the like of the whole coating film can be further improved.

 以上、本発明によって、黒又はそれに近い濃彩色でありながら、近赤外領域での反射特性に優れ、そのため熱エネルギーの吸収が少ない耐候性に優れた塗料を得ることができた。また本発明の塗装方法は、上記塗料の優れた耐候性を最も効果的に引き出すことができる。 As described above, according to the present invention, it was possible to obtain a paint having excellent reflection characteristics in the near-infrared region and having low heat energy absorption and excellent weather resistance while being black or a dark color close thereto. Further, the coating method of the present invention can most effectively bring out the excellent weather resistance of the paint.

 以下、本発明の実施の形態を詳細に説明する。
 本発明の塗料は、可視領域で吸収を示し近赤外領域では反射を示す顔料(以下、濃彩色反射顔料という)を用いることを特徴とする。可視領域で吸収を示すため、従来のカーボンブラック等と同様に、黒色、濃茶色等の濃彩色を呈する。しかし、近赤外領域において光吸収がなく、高い反射率を有するため、熱エネルギーの吸収がなく塗膜の温度上昇を防ぐことができる。そのため塗膜の熱劣化を抑制することができる。
Hereinafter, embodiments of the present invention will be described in detail.
The paint of the present invention is characterized by using a pigment that absorbs in the visible region and reflects in the near-infrared region (hereinafter referred to as a dark-colored reflective pigment). Since it shows absorption in the visible region, it exhibits dark colors such as black and dark brown, similarly to conventional carbon black and the like. However, since there is no light absorption in the near-infrared region and high reflectivity, there is no absorption of heat energy, so that a rise in the temperature of the coating film can be prevented. Therefore, thermal deterioration of the coating film can be suppressed.

 上記の濃彩色反射顔料としては、紫外及び可視領域で吸収を示し近赤外領域で反射を示す顔料であれば特に限定することなく用いることができるが、その中でも、JIS A 5759建築用熱線遮蔽及びガラス飛散防止フィルムで定義される350〜2100nmの領域における日射反射率が15%以上である顔料が好適に用いられる。なお、本特許の日射反射率データは、十分に隠蔽された状態、具体的には隠蔽率が約1.0の塗膜において測定される。 As the above-mentioned dark-colored reflective pigment, any pigment that absorbs in the ultraviolet and visible regions and reflects in the near-infrared region can be used without any particular limitation. Among them, JIS A-5759 Architectural heat ray shielding And a pigment having a solar reflectance of 15% or more in a 350 to 2100 nm region defined by the glass shatterproof film is preferably used. In addition, the solar reflectance data of this patent is measured in a sufficiently concealed state, specifically, a coating film having a concealment ratio of about 1.0.

 また濃彩色反射顔料は、日射反射率が15%以上であると同時に、CIE1976L* a* b* 色空間におけるL* 値が24以下のものを用いる。L* 値が24以下であることは黒色又はそれに近い濃彩色であることを意味する。以上のような条件を満たす顔料の具体例としては、商品名クロモファインブラックA−1103(大日精化工業(株)製)のアゾメチアゾ系顔料、及び焼成顔料等が挙げられる。 濃 Further, as the deep-colored reflective pigment, those having a solar reflectance of 15% or more and an L * value of 24 or less in a CIE1976 L * a * b * color space are used. An L * value of 24 or less means a black color or a dark color close to it. Specific examples of the pigment satisfying the above conditions include azomethiazo pigments manufactured by Chromo Fine Black A-1103 (trade name, manufactured by Dainichi Seika Kogyo Co., Ltd.), and calcined pigments.

 塗料中の濃彩色反射顔料の含有量としては,塗料の用途、耐候性等を考慮して適宜設定することができるが、含有量が少ないと隠蔽力が不足して塗料本来の美観の役割を十分発揮できず、かつ下塗等の劣化を生じやすくなり、逆に含有量が多いと、塗膜が脆くなりかつコストも高くなるため、塗料の樹脂固形分100重量部に対して7〜110重量部が好ましい。 The content of the dark reflective pigment in the paint can be appropriately set in consideration of the use of the paint, weather resistance, etc. However, if the content is small, the hiding power is insufficient, and the role of the original aesthetic of the paint is insufficient. When the content is too high, the coating tends to be brittle and the cost increases. Parts are preferred.

 さらに本発明の遮熱性塗料は、耐候性の優れたビヒクルを用いることを特徴とする。ここでいう耐候性に優れたビヒクルとは、耐黄変性、保色性、光沢保持性、耐薬品性、及び耐白亜化性等に優れたビヒクルをいい、水溶性型及び溶剤型、あるいは常温乾燥型及び焼き付け型のいずれも用いることができる。このようなビヒクルを上述の濃彩色反射顔料と共に用いることにより、塗膜全体としての優れた耐候性を得ることができる。 Furthermore, the heat shielding paint of the present invention is characterized by using a vehicle having excellent weather resistance. The vehicle excellent in weather resistance as referred to herein means a vehicle excellent in yellowing resistance, color retention, gloss retention, chemical resistance, chalking resistance, etc., water-soluble type and solvent type, or at room temperature. Both a drying type and a baking type can be used. By using such a vehicle together with the above-mentioned dark reflective pigment, excellent weather resistance of the entire coating film can be obtained.

 上記の耐候性の優れたビヒクルの具体例としては、その主成分に、アクリル樹脂、ポリエステル樹脂、シリコン変性ポリエステル樹脂、シリコン変性アクリル樹脂、アルキッド樹脂、塩化ビニル樹脂、及びフッ素系樹脂等を用いたものを挙げることができ、その中でもポリエステル樹脂、フッ素系樹脂は好適に用いられる。また必要に応じ、各種イソシアネート、メラミン樹脂等の硬化剤を用いることができる。 As specific examples of the above-mentioned vehicle having excellent weather resistance, the main components thereof were acrylic resin, polyester resin, silicon-modified polyester resin, silicon-modified acrylic resin, alkyd resin, vinyl chloride resin, and fluorine-based resin. Among them, polyester resins and fluorine-based resins are preferably used. If necessary, a curing agent such as various isocyanates and melamine resins can be used.

 本発明の塗料には、上記の濃彩色反射顔料に加えて、カーボンブラックや鉄黒等の従来の黒色顔料を除いた着色顔料を少なくとも一種以上と、白色顔料(以下、着色顔料等という)とを含有することができる。白色顔料は必要に応じて用いればよく、したがって濃彩色反射顔料以外の顔料として、着色顔料のみの場合と着色及び白色顔料を用いる場合が適用可能である。着色顔料等を含有することによって様々な色の塗料を調整することができる。従来のカーボンブラック等の黒色顔料を混色する場合に比較すると、塗膜の熱エネルギーの吸収が少ないため変退色等が起こりにくい。 In the paint of the present invention, in addition to the above-mentioned dark reflective pigment, at least one or more coloring pigments excluding conventional black pigments such as carbon black and iron black, and white pigments (hereinafter, referred to as coloring pigments and the like) Can be contained. The white pigment may be used as needed. Therefore, as a pigment other than the deeply colored reflective pigment, a case of using only a colored pigment and a case of using a colored and white pigment are applicable. By containing coloring pigments and the like, paints of various colors can be adjusted. Compared to a conventional case where a black pigment such as carbon black is mixed, the coating film absorbs less heat energy, so that discoloration and the like hardly occur.

 上記着色顔料としては、通常用いられる各種顔料が適用可能であるが、その中でも、JIS A 5759に定義される350〜2100nmの領域における日射反射率が12%以上の顔料が好適に用いられる。なお、本特許の日射反射率データは十分に隠蔽された塗膜において測定される。この条件を満たす着色顔料の例としては、モノアゾ系エロー(商品名ホスターパームエローH3G:ヘキスト(株)製)等の黄色系顔料、酸化鉄(商品名トダカラー120ED:戸田工業(株)製)、キナクリドンレッド(Hostaperm Red E2B70:ヘキスト(株)製)等の赤色系顔料、フタロシアニンブルー(商品名シヤニンブルーSPG−8:大日本インキ(株)製)等の青色系顔料、フタロシヤニングリーン(商品名シヤニングリーン5310:大日精化工業(株)製)等の緑色系顔料等が挙げられる。 As the above-mentioned coloring pigment, various kinds of commonly used pigments can be applied. Among them, pigments having a solar reflectance of 12% or more in a 350 to 2100 nm region defined in JIS A # 5759 are preferably used. It should be noted that the solar reflectance data of this patent is measured on fully concealed coatings. Examples of the coloring pigment satisfying this condition include yellow pigments such as monoazo yellow (trade name Hoster Palm Yellow H3G: manufactured by Hoechst Co., Ltd.), iron oxide (trade name: Todacolor 120ED, manufactured by Toda Kogyo Co., Ltd.), Red pigments such as quinacridone red (Hostaperm Red E2B70: manufactured by Hoechst Co., Ltd.), blue pigments such as phthalocyanine blue (trade name: Cyanin Blue SPG-8: Dainippon Ink Co., Ltd.), and phthalocyanine green (trade name) Green pigments such as cyanine green 5310 (manufactured by Dainichi Seika Kogyo Co., Ltd.).

 また前記白色顔料としても、特に限定されるものではなく、具体例として酸化チタン、亜鉛華等の顔料を適宜用いることができる。酸化チタンはルチル型、アナターゼ型共に適用可能であるが、ルチル型の酸化チタンが特に好適に用いられる。 Also, the white pigment is not particularly limited, and specific examples thereof include pigments such as titanium oxide and zinc white. Titanium oxide can be applied to both rutile type and anatase type, but rutile type titanium oxide is particularly preferably used.

 濃彩色反射顔料と着色顔料等を組み合わせて用いる場合の含有量は、塗料の樹脂固形分100重量部に対してそれぞれ、濃彩色反射顔料を7〜110重量部、着色顔料を7〜110重量部、及び白色顔料を40〜230重量部とすることが好ましい。これ以外の範囲では、含有量が少ないと隠蔽力が不足し、含有量が多いと塗装作業性、耐久性に劣るため不適当である。 The content in the case of using a combination of a dark reflective pigment and a colored pigment is 7 to 110 parts by weight of the dark reflective pigment and 7 to 110 parts by weight of the colored pigment with respect to 100 parts by weight of the resin solid content of the paint. , And 40 to 230 parts by weight of a white pigment. If the content is outside the above range, the concealing power is insufficient if the content is small, and the coating workability and durability are poor if the content is large.

 また顔料全体としての含有量は、塗料の樹脂固形分100重量部に対して7〜150重量部とすることが好ましい。含有量は所定の量より少ないと、塗膜の隠蔽力が十分に得られず太陽光等が透過しやすくなるため温度上昇が起こり塗膜劣化の原因となる。また隠蔽力を得るため膜厚を厚くすると塗装作業性に支障をきたすため不適当である。逆に所定の量より多いと、塗膜表面の顔料が一部むき出しになるため平滑度が低下し、水分、光、熱等に対する耐性も著しく損なわれるため不適当である。 (4) The content of the pigment as a whole is preferably 7 to 150 parts by weight based on 100 parts by weight of the resin solid content of the paint. If the content is less than the predetermined amount, sufficient hiding power of the coating film cannot be obtained, and sunlight and the like are easily transmitted, so that the temperature rises and causes deterioration of the coating film. On the other hand, if the film thickness is increased to obtain the hiding power, the coating workability is impaired, which is not suitable. Conversely, if the amount is larger than the predetermined amount, the pigment on the surface of the coating film is partially exposed, so that the smoothness is lowered, and the resistance to moisture, light, heat and the like is significantly impaired.

 塗料化するための分散工程における、上記の濃彩色反射顔料及び着色顔料等の分散度は、塗料の種類、用途等によって設定することができ特に限定されるものではないが、平均粒子径が50μm以下になるように分散することが好ましく、10μm以下が最も好ましい。50μm以上であると、塗膜表面が凸凹になり外観を損なうと共に、粗い塗膜表面に塵埃等が付着しやすくなり、塗膜温度が上がりやすくなって耐候性、耐汚染性、色安定性等が悪化するため不適当である。 In the dispersing step for forming a paint, the degree of dispersion of the above-described dark-colored reflective pigments and colored pigments can be set according to the type of the paint, the use, etc., and is not particularly limited, but the average particle diameter is 50 μm. It is preferable that the particles be dispersed so as to be less than or equal to 10 μm. When the thickness is 50 μm or more, the surface of the coating film becomes uneven and the appearance is impaired, and dust and the like easily adhere to the rough coating film surface, and the coating film temperature easily rises, resulting in weather resistance, stain resistance, color stability, and the like. Is unsuitable because it deteriorates.

 顔料を分散させる際に用いる分散媒体としては鉄以外のものを用いることが好ましい。鉄製の分散媒体は着色汚染によって顔料の日射反射率を低下させるため不適当である。鉄以外の分散媒体の具体例としては、陶磁製、ガラスビーズ、フリント石等が挙げられ、この中でもガラスビーズは容易に入手可能であり経済性にも優れるため好適に用いられる。分散媒体の粒度、充填量、及び顔料分散機の種類等は特に限定されるものではないが、実施形態の具体例として、3〜1.5mmのガラスビーズをサンドグラインドミル容量の約80%充填する場合を挙げることができる。 と し て It is preferable to use a medium other than iron as a dispersion medium used for dispersing the pigment. Iron dispersion media are unsuitable because they reduce the solar reflectance of the pigment due to color contamination. Specific examples of the dispersion medium other than iron include ceramics, glass beads, flint stone, and the like. Among them, glass beads are easily used and excellent in economical efficiency, and thus are preferably used. The particle size of the dispersing medium, the filling amount, the type of the pigment dispersing machine, etc. are not particularly limited. However, as a specific example of the embodiment, glass beads of 3 to 1.5 mm are filled to about 80% of the capacity of the sand grind mill. Can be mentioned.

 本発明の遮熱性塗料には上記の顔料及びビヒクルに加えて、反射機能及び断熱機能を有する骨材を含有することができる。骨材の具体例としてはシラスバルーン、ポリスチレンバルーン、セラミックバルーン等の中空粒子が挙げられる。これらの骨材は反射機能及び断熱機能を有するため上述の濃彩色反射顔料とあいまって、塗膜の遮熱性、耐候性をさらに向上させることができる。 熱 In addition to the pigment and the vehicle, the heat-shielding paint of the present invention may contain an aggregate having a reflecting function and a heat insulating function. Specific examples of the aggregate include hollow particles such as shirasu balloons, polystyrene balloons, and ceramic balloons. Since these aggregates have a reflecting function and a heat insulating function, they can further improve the heat shielding property and the weather resistance of the coating film in combination with the above-mentioned deeply colored reflecting pigment.

 上記の添加剤の中でも、ホウ化ケイ素系等のセラミックバルーンはその表層及び殻内で太陽光等を反射することができ、中空で断熱性にも優れているため好適に用いられる。さらに、セラミックバルーンは、構造保持剤と共に用いることが好ましい。ここで述べるセラミックバルーン及び構造保持剤を含有する塗料については、本発明者らが特願平10−130742号で既に提案したものである。セラミックバルーンは比重が1より小さいため単独で用いた場合には塗料の表面に浮きやすくなり、そのため塗料表層の溶剤が揮発していわゆる皮張り現象を起こし、貯蔵安定性が悪くなるという問題があるが、構造保持剤を含有させることによって、塗料中に構造粘性が付与され、バルーンを均一に分布させることができ、貯蔵安定性は向上する。またバルーンを含有する塗膜は耐水性を有するため総合的な耐候性をさらに向上することができる。 Among the above additives, silicon boride ceramic balloons and the like are preferably used because they can reflect sunlight and the like in the surface layer and in the shell, and are hollow and excellent in heat insulation. Further, the ceramic balloon is preferably used together with a structure retaining agent. The paint containing the ceramic balloon and the structure retaining agent described herein has already been proposed by the present inventors in Japanese Patent Application No. 10-130742. Since the ceramic balloon has a specific gravity of less than 1, when it is used alone, it tends to float on the surface of the coating, so that the solvent in the coating surface layer volatilizes, causing a so-called skinning phenomenon, which causes a problem of poor storage stability. However, by including the structure-retaining agent, structural viscosity is imparted to the paint, the balloon can be uniformly distributed, and the storage stability is improved. Further, since the coating film containing the balloon has water resistance, the overall weather resistance can be further improved.

 本発明において適用可能な、セラミックバルーン及び構造保持剤の種類、含有量等の条件は特願平10−130742号で開示する条件と同様であるが、それに加えて濃彩色反射顔料との相乗効果により最適な耐候性を得るために以下の条件が好ましく用いられる。すなわち、バルーンの粒子径は5〜110μmが好ましい。110μmより大きいと塗膜が凸凹になるため不適当である。粒径分布は累計50%領域で30〜65μm、90%累計で50〜110μmが好ましい。またバルーンの比重は0.16〜0.6が好ましい。さらにバルーンの強度は20〜750kgf/cm2 の範囲が好ましい。この範囲より小さいとバルーンが塗料製造時に破壊されやすく、逆に大きいとバルーンの殻が厚くなり遮熱効果が低下するため不適当である。さらに構造保持剤の種類としては、脂肪酸アマイド/微粒シリカの複合系、有機ベントナイト/微粒シリカの複合系、及び脂肪酸アマイド/有機ベントナイト/微粒シリカの複合系、酸化ポリエチレンワックス/微粒シリカの複合系、及び上記複合系から微粒シリカを除いたもの等が好適に用いられる。 The conditions applicable to the present invention, such as the type and content of the ceramic balloon and the structure-retaining agent, are the same as those disclosed in Japanese Patent Application No. 10-130742. In order to obtain more optimal weather resistance, the following conditions are preferably used. That is, the particle diameter of the balloon is preferably 5 to 110 μm. If it is larger than 110 μm, the coating film becomes uneven, which is not suitable. The particle size distribution is preferably 30 to 65 μm in a 50% cumulative area, and 50 to 110 μm in a 90% cumulative area. The specific gravity of the balloon is preferably from 0.16 to 0.6. Further, the strength of the balloon is preferably in the range of 20 to 750 kgf / cm 2 . If it is smaller than this range, the balloon is liable to be destroyed during the production of the coating material. Further, as the type of the structure retaining agent, a complex system of fatty acid amide / fine silica, a complex system of organic bentonite / fine silica, a complex system of fatty acid amide / organic bentonite / fine silica, a composite system of polyethylene oxide / fine silica, And those obtained by removing fine silica from the above composite system are preferably used.

 さらに、本発明の塗料は、通常用いられる種々の添加剤を含有することができる。具体的には、色分かれ防止剤、沈殿防止剤、表面調整剤、潤滑剤、可塑剤、消泡剤、防腐剤、凍結防止剤、硬化剤、顔料分散剤、乳化剤、乾燥剤、紫外線吸収剤、防かび剤、抗菌剤等が挙げられる。 塗料 Furthermore, the coating material of the present invention can contain various additives which are usually used. Specifically, color separation preventives, sedimentation preventives, surface conditioners, lubricants, plasticizers, defoamers, preservatives, antifreezes, hardeners, pigment dispersants, emulsifiers, desiccants, ultraviolet absorbers , Fungicides, antibacterial agents and the like.

 以上の塗料を塗布する素材としては特に限定されるものではなく、木材、コンクリート、アスベスト、金属、樹脂等の種々の素材が選択可能である。また塗布する用途は、遮熱機能を付与したい場所であれば適用でき、例えば家、工場、保冷倉庫等の建築物や、車、電車、ベンチ、冷凍車等の輸送車、貯蔵タンク、タンカー等の構造物の屋根、天井、外壁、内壁等が挙げられる。 素材 The material to which the above paint is applied is not particularly limited, and various materials such as wood, concrete, asbestos, metal, and resin can be selected. In addition, the application for application can be applied to places where it is desired to provide a heat-shielding function, for example, buildings such as houses, factories, cold storage warehouses, transportation vehicles such as cars, trains, benches, and freezing vehicles, storage tanks, tankers, and the like. Roof, ceiling, outer wall, inner wall, etc.

 塗布する方法としては、目的に応じ適宜選択すれば良く、具体的にはハケ塗り、ローラー塗り、スプレー、ロールコーター塗装等が挙げられる。塗布する対象物によっては、静電塗装、カーテン塗装、浸漬法等も適用可能である。さらに塗布後、乾燥させて塗膜化させる方法についても、自然乾燥、焼き付け等の方法を用いることができ塗料の性状によって適宜選択される。 方法 The method of coating may be appropriately selected according to the purpose, and specific examples include brush coating, roller coating, spraying, and roll coater coating. Depending on the object to be coated, electrostatic coating, curtain coating, dipping, and the like are also applicable. Further, a method of drying and forming a coating film after application can be appropriately selected depending on the properties of the coating material, such as natural drying and baking.

 塗膜の膜厚は、塗料や素材の性状等によって適宜設定することができるが、8μm以上になるように塗装することが好ましく、10μm以上がより好ましい。8μm以下であると隠蔽力が不足し、またセラミックバルーンを含有する場合にはバルーンが不均一に分布して十分な遮熱性能が得られない傾向がある。逆に厚すぎると、焼き付け塗料の場合はピンホールが発生し、常乾型の場合は塗料のタレが発生するため、不適当である。 膜厚 The thickness of the coating film can be appropriately set depending on the properties of the coating material and the material, but it is preferable to apply the coating so as to have a thickness of 8 μm or more, and more preferably 10 μm or more. When the thickness is less than 8 μm, the hiding power is insufficient, and when the ceramic balloon is contained, the balloon tends to be non-uniformly distributed and sufficient heat shielding performance cannot be obtained. On the other hand, if the thickness is too large, pinholes occur in the case of a baked paint, and in the case of a normal dry type, the paint sags.

 さらに、本発明の塗料を素材に塗布するにあたっては、予め下塗りを施すことができる。下塗りは、錆止めや、本発明の塗料の素材との付着性向上、また上塗り塗料との付着性向上を目的として行われ、従来知られた下塗り塗料を適宜用いることができる。具体的な下塗り塗料の種類としては、エポキシ樹脂、アルキッド樹脂、エポキシウレタン系樹脂、ポリエステル樹脂等の樹脂に、酸化チタン、防錆顔料、体質顔料等を添加したもの等が好適に用いられる。塗膜厚は素材、上塗りの種類、要求性能等を考慮して適宜決めることができる。下塗りを施すことにより本発明の塗料の付着性が高まり、塗膜の耐久性を向上させ、上塗りの適用範囲を広げることができる。 Furthermore, when applying the paint of the present invention to a material, a primer can be applied in advance. The undercoating is performed for the purpose of preventing rust, improving the adhesion of the paint of the present invention to the material, and improving the adhesion to the overcoat, and a conventionally known undercoat can be appropriately used. As a specific type of the undercoat paint, a resin obtained by adding titanium oxide, a rust preventive pigment, an extender pigment, or the like to a resin such as an epoxy resin, an alkyd resin, an epoxy urethane resin, or a polyester resin is preferably used. The thickness of the coating film can be appropriately determined in consideration of the material, type of overcoat, required performance, and the like. By applying the undercoat, the adhesion of the paint of the present invention is enhanced, the durability of the coating film is improved, and the application range of the overcoat can be expanded.

 また、本発明の塗料を塗布した後に汚染防止用クリヤー等の上塗りを施すことができる。上塗りによって、塗膜の付着性、耐水性等を向上させることができ、また大気中の塵埃による汚染を防止し日射反射率の低下を防ぐことができる。さらに艶あり塗膜を提供することができる。上塗り塗料としては、アクリル系、ポリエステル系の汚染防止用クリヤー等が適用可能であり、特に紫外線防止剤を添加したり、沈降性硫酸バリウム等の体質顔料を分散添加した有機無機複合系樹脂は、汚染防止効果が優れており好適に用いられる。さらに、上塗りの膜厚は、本発明の塗料を完全に覆うことができれば特に限定されるものではないが、5〜50μm程度とすることが好ましい。 後 に Furthermore, after applying the paint of the present invention, a top coat such as a stain prevention clear can be applied. The overcoating can improve the adhesion and water resistance of the coating film, and can prevent contamination by dust in the atmosphere and prevent a decrease in solar reflectance. Further, a glossy coating film can be provided. As the overcoat paint, acrylic-based, polyester-based stain-preventing clears and the like are applicable.In particular, an organic-inorganic composite resin to which an anti-UV agent is added or an extender pigment such as precipitated barium sulfate is dispersed and added, It has an excellent effect of preventing contamination and is suitably used. Further, the thickness of the overcoat is not particularly limited as long as it can completely cover the paint of the present invention, but is preferably about 5 to 50 μm.

 上記の下塗り及び上塗りは、一方のみを施すこともできるし、両方施すこともできる。また、必要に応じて中塗りを施すこともできる。中塗りは塗膜を厚くするため、耐食性を向上させたり、塗膜のわれ、剥離等に対する耐性を付与する効果を有する。どのような塗装系とするかは、用途、要求性能(耐久性、耐候性)、経済性等を考慮して適宜選択される。 The above-mentioned undercoat and overcoat can be applied alone or both. Further, an intermediate coating can be applied as necessary. The intermediate coating has the effect of improving corrosion resistance and imparting resistance to cracking, peeling, and the like of the coating because the coating is thick. What kind of coating system is used is appropriately selected in consideration of the application, required performance (durability, weather resistance), economy, and the like.

 以下、実施例及び比較例により本発明をさらに具体的に説明するが、これによって限定されるものではない。 Hereinafter, the present invention will be described more specifically with reference to Examples and Comparative Examples, but the present invention is not limited thereto.

1.原料
 実施例で作製した塗料の原料を表1に示す。
1. Raw materials Table 1 shows the raw materials of the coating materials prepared in the examples.

Figure 2004027241
Figure 2004027241

2.塗料の作製
 (1)原料を表2に示す割合で、まず樹脂L、溶剤、及び各顔料を混合した後、樹脂N、消泡剤Qを加え粘度70±5KUに調整しG1〜G8とした。なお、顔料は10μm以下に分散させ、その際の分散媒体は粒度2.1mmのガラスビーズ(商品名:ハイビーD10)を用いた。分散工程は、分散媒体500g、プレミックスペースト300gを卓上型バッチ式SGミルを用いて分散した。
2. Preparation of paint (1) After mixing the raw materials in the ratio shown in Table 2, first, resin L, solvent, and each pigment were mixed, resin N and defoamer Q were added to adjust the viscosity to 70 ± 5 KU to obtain G1 to G8. . The pigment was dispersed to 10 μm or less, and the dispersion medium used was glass beads having a particle size of 2.1 mm (trade name: Hibee D10). In the dispersion step, 500 g of the dispersion medium and 300 g of the premix paste were dispersed by using a table-top batch type SG mill.

Figure 2004027241
Figure 2004027241

 (2)G1〜G8及び樹脂等を表3に示す割合で混合し、塗料サンプルP1〜P3、C1、及びC2を得た。 (2) G1 to G8, resin, and the like were mixed at the ratios shown in Table 3 to obtain paint samples P1 to P3, C1, and C2.

Figure 2004027241
Figure 2004027241

3.試験板の作製
 表2、表3の塗料を用い、表4の塗板作製条件にて試験板を作製した。なお、下塗り塗料は、エポキシウレタン系樹脂、酸化チタン、防錆顔料、及び体質顔料からなるものである。また上塗り塗料は、表3におけるP3である。さらに、塗装方法はバーコーターで行い、焼き付けは電熱対流炉で行った。焼き付け条件は以下の通りである。
下塗り 炉温150℃×15分
本塗料 炉温150℃×20分
クリヤー 炉温150℃×20分
3. Preparation of Test Plate Using the paints in Tables 2 and 3, test plates were prepared under the coating plate preparation conditions in Table 4. The undercoat paint is composed of an epoxy urethane resin, titanium oxide, a rust preventive pigment, and an extender pigment. The top coat is P3 in Table 3. Further, the coating method was performed by a bar coater, and the baking was performed by an electric convection oven. The printing conditions are as follows.
Undercoat Furnace temperature 150 ° C × 15 minutes Main paint Furnace temperature 150 ° C × 20 minutes Clear Furnace temperature 150 ° C × 20 minutes

4.試験方法
 (1)反射率チャート
 反射率の波長依存性を分光光度計を用いて測定した。測定結果を図1〜12に示す。
 (2)日射反射率
 塗膜の日射反射率を、JIS A 5759に定義される350〜2100nmの領域における日射反射率として測定した。その結果を表4に示す。
 (3)L* 値
 CIE1976L* a* b* 色空間におけるL* を、カラコムC型分光光度 計(大日精化工業(株)製)によって測定した。その結果を表4に示す。
 (4)塗板温度
 ランプ照射による塗板温度を測定した。まず、図13に示すようなコの字形の塗板1を成型し、成型品2つを幅方向に並べ200Wの東芝レフランプを塗板より130mmの高さから照射した。なお、図13中のa、b、及びcは成型品の寸法を表し、それぞれa=220mm、b=110mm、c=45mmである。塗板の温度は塗板の裏側中央に取り付けた温度センサー2で測定した。温度は、ランプ照射開始15〜20分でほぼ一定になるので20分後の温度を測定値とした。測定結果を表4に示す。
 (5)QUV1900時間
 促進曝露試験機QUVにて1900時間照射した後のΔE* を測定した。測定結果を表4に示す。
 (6)カーボン汚染テスト
 5%カーボン顔料水溶液を塗膜に塗布し20℃で24時間放置後、水洗いしながらスポンジたわしで軽くこすりカーボンを落とす。テスト前後の色差をΔL* 値として測定した。測定結果を表4に示す。
 (7)5%NaOHテスト
 20℃の5%NaOH水溶液に、試験板を24時間浸漬し、その後の塗膜状態を観察した。観察結果を以下の判定基準で評価した。
○ 異常無し
△ 塗膜に若干ブリスター有り
× 塗膜に著しくブリスター有り
 (8)表5で示した配合で塗料1kgを作製し、その塗料を容器に入れ、2週間静置した後、塗料状態を観察した。その結果を以下の判定基準で評価した。
◎ バルーンの表層浮きがなく良好
○ バルーンの表層浮きが若干あるが実用性に問題なし
× バルーンの表層浮きがあり実用上問題あり
4. Test method (1) Reflectance chart The wavelength dependence of the reflectance was measured using a spectrophotometer. The measurement results are shown in FIGS.
(2) Solar reflectance The solar reflectance of the coating film was measured as the solar reflectance in the range of 350 to 2100 nm defined in JIS A 5759. Table 4 shows the results.
(3) L * value L * in the CIE1976 L * a * b * color space was measured with a Karacom C-type spectrophotometer (manufactured by Dainichi Seika Kogyo Co., Ltd.). Table 4 shows the results.
(4) Coated plate temperature The coated plate temperature by lamp irradiation was measured. First, a U-shaped coated plate 1 as shown in FIG. 13 was molded, two molded products were arranged in the width direction, and a 200 W Toshiba reflex lamp was irradiated from a height of 130 mm from the coated plate. In addition, a, b, and c in FIG. 13 represent the dimensions of the molded product, and are a = 220 mm, b = 110 mm, and c = 45 mm, respectively. The temperature of the coated plate was measured by the temperature sensor 2 attached to the center of the back side of the coated plate. Since the temperature became almost constant 15 to 20 minutes after the start of lamp irradiation, the temperature after 20 minutes was used as the measured value. Table 4 shows the measurement results.
(5) QUV 1900 hours ΔE * was measured after irradiation with an accelerated exposure tester QUV for 1900 hours. Table 4 shows the measurement results.
(6) Carbon contamination test A 5% aqueous solution of carbon pigment is applied to the coating film, left at 20 ° C. for 24 hours, and gently rubbed with a sponge scourer while washing with water to remove carbon. The color difference before and after the test was measured as ΔL * value. Table 4 shows the measurement results.
(7) 5% NaOH test The test plate was immersed in a 5% NaOH aqueous solution at 20 ° C. for 24 hours, and the state of the subsequent coating film was observed. The observation results were evaluated according to the following criteria.
○ There is no abnormality. There is some blister in the coating film. X There is remarkable blister in the coating film. (8) Prepare 1 kg of paint with the composition shown in Table 5, put the paint in a container, and let it stand for 2 weeks. Observed. The results were evaluated according to the following criteria.
◎ Good with no balloon surface floating ○ Good balloon surface floating but no problem in practicality × Balloon surface floating and practically problematic

Figure 2004027241
Figure 2004027241
Figure 2004027241
Figure 2004027241

 以上の結果より、本発明の塗料は、従来の黒色顔料を使用した場合に比較して、塗板温度を10℃以上低く抑えることができ、QUV測定から耐候性に優れていることが明らかとなった。このことは反射率チャートの近赤外領域において、本発明の塗料の反射率が大きいことからも示唆される。 From the above results, it is clear that the coating material of the present invention can keep the coating plate temperature lower by 10 ° C. or more as compared with the case where the conventional black pigment is used, and is excellent in weather resistance from QUV measurement. Was. This is suggested from the fact that the paint of the present invention has a large reflectance in the near infrared region of the reflectance chart.

 また、セラミックバルーン及び構造保持剤を含有させることにより、表4のE12及びE13からわかるように、反射性能、及び耐候性が向上することが明らかである。 Also, as can be seen from E12 and E13 in Table 4, it is clear that the inclusion of the ceramic balloon and the structure retaining agent improves the reflection performance and the weather resistance.

 さらに表4のE7とE8、及びE9とE11を比較して、汚染防止用クリヤー等の上塗りを施すことによって、耐汚染性、耐候性等が向上することが明らかである。 Further, by comparing E7 and E8 and E9 and E11 in Table 4, it is clear that by applying a top coat such as a stain prevention clear, the stain resistance and weather resistance are improved.

 さらに表4のE16より、分散媒体として鉄を用いると遮熱性が劣化することが明らかである。 Furthermore, from E16 in Table 4, it is clear that when iron is used as the dispersion medium, the thermal barrier properties deteriorate.

 また表5から、構造保持剤は、バルーンの浮きを防ぎ、貯蔵安定性を大きく向上させることが明らかである。 Also, from Table 5, it is clear that the structure retaining agent prevents the balloon from floating and greatly improves the storage stability.

サンプルE1における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E1. サンプルE2における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E2. サンプルE3における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E3. サンプルE4における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E4. サンプルE5における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E5. サンプルE6における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E6. サンプルE7における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E7. サンプルE12における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E12. サンプルE13における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E13. サンプルE14における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E14. サンプルE15における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E15. サンプルE16における反射率の波長依存性を示すグラフである。It is a graph which shows the wavelength dependence of the reflectance in sample E16. ランプの照射方法を示す図である。It is a figure showing the irradiation method of a lamp.

符号の説明Explanation of reference numerals

1 塗板
2 温度センサー
a 成型品の寸法
b 成型品の寸法
c 成型品の寸法
1 Painted plate 2 Temperature sensor a Molded product dimension b Molded product dimension c Molded product dimension

Claims (10)

 可視領域で吸収を示し近赤外領域では反射を示す顔料と、耐候性に優れるビヒクルとを含有することを特徴とする遮熱性塗料。 (4) A heat-shielding paint comprising a pigment that absorbs in the visible region and reflects in the near-infrared region, and a vehicle having excellent weather resistance.  前記顔料が、JIS A 5759に定義される日射反射率が15%以上であって、かつCIE1976L* a* b* 色空間におけるL* 値が24以下の顔料であることを特徴とする請求項1記載の遮熱性塗料。 2. The pigment according to claim 1, wherein the pigment has a solar reflectance defined by JIS A-5759 of 15% or more and an L * value of 24 or less in a CIE1976 L * a * b * color space. The heat-shielding paint as described.  前記顔料の含有量が、塗料の樹脂固形分100重量部に対して7〜110重量部であることを特徴とする請求項1又は2記載の遮熱性塗料。 (3) The heat-shielding paint according to (1) or (2), wherein the content of the pigment is 7 to 110 parts by weight based on 100 parts by weight of the resin solid content of the paint.  前記顔料に加えて、JIS A 5759に定義される日射反射率が12%以上である着色顔料を少なくとも一種以上と、必要に応じて白色顔料とを含有することを特徴とする請求項1乃至3記載の遮熱性塗料。 4. The ink composition according to claim 1, further comprising, in addition to the pigment, at least one color pigment having a solar reflectance of 12% or more as defined in JIS A-5759, and optionally a white pigment. The heat-shielding paint as described.  請求項1乃至3記載の顔料、前記着色顔料、及び前記白色顔料の含有量が、塗料の樹脂固形分100重量部に対して、それぞれ7〜110重量部、7〜110重量部、及び40〜230重量部であることを特徴とする請求項4記載の遮熱性塗料。 The content of the pigment according to any one of claims 1 to 3, the color pigment, and the white pigment is 7 to 110 parts by weight, 7 to 110 parts by weight, and 40 to 100 parts by weight, respectively, based on 100 parts by weight of the resin solid content of the coating material. The heat-shielding paint according to claim 4, wherein the amount is 230 parts by weight.  前記白色顔料が、酸化チタン顔料であることを特徴とする請求項4又は5記載の遮熱性塗料。 6. The heat-shielding paint according to claim 4, wherein the white pigment is a titanium oxide pigment.  前記顔料は、塗料中において平均粒子径が50μm以下に分散されていることを特徴とする請求項1乃至6記載の遮熱性塗料。 (7) The heat-shielding paint according to any one of (1) to (6), wherein the pigment is dispersed in the paint to have an average particle size of 50 μm or less.  セラミックバルーン及び構造保持剤を含有することを特徴とする請求項1乃至7記載の遮熱性塗料。 8. The heat-shielding paint according to claim 1, further comprising a ceramic balloon and a structure-retaining agent.  耐候性に優れるビヒクルが、アクリル樹脂、ポリエステル樹脂、シリコン変性ポリエステル樹脂、シリコン変性アクリル樹脂、アルキッド樹脂、塩化ビニル樹脂、及びフッ素系樹脂の少なくとも一種以上と、必要に応じ、イソシアネート、メラミン樹脂の少なくとも一種以上とを含有することを特徴とする請求項1乃至8記載の遮熱性塗料。 A vehicle having excellent weather resistance is an acrylic resin, a polyester resin, a silicon-modified polyester resin, a silicon-modified acrylic resin, an alkyd resin, a vinyl chloride resin, and at least one of a fluororesin, and, if necessary, at least one of an isocyanate and a melamine resin. 9. The heat-shielding paint according to claim 1, comprising one or more kinds.  請求項1乃至9記載の遮熱性塗料を、塗膜厚が8μm以上になるように塗装し、必要に応じて、下塗り及び/又は上塗りを施すことを特徴とする遮熱性塗料の塗装方法。 (10) A method for coating a heat-shielding paint, comprising applying the heat-shielding paint according to any one of claims 1 to 9 so that the coating film thickness is 8 µm or more, and applying an undercoat and / or an overcoat as needed.
JP2003354259A 2003-10-14 2003-10-14 Thermal insulation coating and its coating method Pending JP2004027241A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2003354259A JP2004027241A (en) 2003-10-14 2003-10-14 Thermal insulation coating and its coating method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2003354259A JP2004027241A (en) 2003-10-14 2003-10-14 Thermal insulation coating and its coating method

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP30596898A Division JP3794837B2 (en) 1998-10-27 1998-10-27 Thermal barrier paint and coating method thereof

Publications (1)

Publication Number Publication Date
JP2004027241A true JP2004027241A (en) 2004-01-29

Family

ID=31185632

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003354259A Pending JP2004027241A (en) 2003-10-14 2003-10-14 Thermal insulation coating and its coating method

Country Status (1)

Country Link
JP (1) JP2004027241A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006015193A (en) * 2004-06-30 2006-01-19 Dainippon Ink & Chem Inc Coating film forming method
WO2009125478A1 (en) * 2008-04-09 2009-10-15 Sci-Paint Japan株式会社 Thermal insulation coating material
JP2009286862A (en) * 2008-05-28 2009-12-10 Nippon Paint Co Ltd Heat-insulating coating material composition, method for forming heat-insulating coating film using the same and heat-insulating coating film
WO2010106890A1 (en) 2009-03-17 2010-09-23 東洋アルミニウム株式会社 Method for reflecting infrared light
CN101531863B (en) * 2009-04-21 2011-09-28 厦门双瑞船舶涂料有限公司 A low solar absorbing energy-saving type neutral gray hull finish coat
CN104250513A (en) * 2014-09-25 2014-12-31 南京理工大学 Yellow-brown near-infrared reflection type thermal-insulating coating and preparation method thereof
CN104250514A (en) * 2014-09-25 2014-12-31 南京理工大学 Deep brown near-infrared reflection type heat insulation coating and preparation method thereof
CN105368180A (en) * 2015-11-23 2016-03-02 安徽酉阳防水科技有限公司 Building insulation exterior wall heat-insulation paint having strong crack-resistance performance

Citations (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3577379A (en) * 1969-03-11 1971-05-04 Us Army Dark colored coatings of high solar heat reflectance
US3700397A (en) * 1969-05-06 1972-10-24 Us Army Camouflaged article and method of producing same
JPS4848529A (en) * 1971-10-25 1973-07-10
JPS5430221A (en) * 1977-08-11 1979-03-06 Dainichi Seika Kogyo Kk Preparation of azo pigments
JPS54141821A (en) * 1978-04-27 1979-11-05 Dainichi Seika Kogyo Kk Azo pigment
JPS54150498A (en) * 1978-05-18 1979-11-26 Mitsui Petrochem Ind Ltd Epoxy resin composition
JPS5527272A (en) * 1978-08-19 1980-02-27 Jirou Takei Method of producing heat shielding metal face plate
JPS5649757A (en) * 1980-08-01 1981-05-06 Dainichi Seika Kogyo Kk Azo pigment
JPS5655456A (en) * 1980-08-01 1981-05-16 Dainichi Seika Kogyo Kk Azo pigment
JPS56109257A (en) * 1980-01-22 1981-08-29 Aburamobuna Shiyuterun Maria Heat reflective enamel
JPS58167642A (en) * 1982-03-08 1983-10-03 ザ・ビー・エフ・グッドリッチ・カンパニー Infrared ray reflective vinyl polymer composition
JPS58174446A (en) * 1982-04-07 1983-10-13 Dainichi Seika Kogyo Kk Azo pigment and its preparation
JPS60149666A (en) * 1984-01-17 1985-08-07 Dainichi Seika Kogyo Kk Azo pigment and production thereof
US4624710A (en) * 1985-09-30 1986-11-25 Harshaw/Filtrol Partnership Pigment consisting of a mixture of chromium oxide and iron oxide useful in high infra red reflectance gray vinyl composition
JPS6230202A (en) * 1985-08-01 1987-02-09 Dainichi Color & Chem Mfg Co Ltd Infrared reflective material
JPS6232149A (en) * 1986-03-07 1987-02-12 Dainichi Color & Chem Mfg Co Ltd Azo compound and colored composition
JPS6268858A (en) * 1985-09-20 1987-03-28 Dainichi Color & Chem Mfg Co Ltd Infrared-reflective material
JPS6268855A (en) * 1985-09-20 1987-03-28 Dainichi Color & Chem Mfg Co Ltd Infrared-reflective material
JPS6279257A (en) * 1985-10-01 1987-04-11 Mitsubishi Heavy Ind Ltd Lightweight, heat insulating coating material
JPS62138857A (en) * 1985-12-12 1987-06-22 Dainichi Color & Chem Mfg Co Ltd Coloring composition for recording image
JPS6391283A (en) * 1986-10-07 1988-04-21 Dainichi Color & Chem Mfg Co Ltd Printed matter and production thereof
JPS63223076A (en) * 1987-03-13 1988-09-16 Seiko Epson Corp Titanium oxide-containing coating compound and coating film
JPS63275682A (en) * 1987-05-07 1988-11-14 Seiko Epson Corp Coating composition containing titanium oxide
JPH01126376A (en) * 1987-11-12 1989-05-18 Nippon Steel Chem Co Ltd Solar-heat shielding coated structure
JPH01263163A (en) * 1988-04-15 1989-10-19 Nippon Steel Chem Co Ltd Solar heat-shielding coating composition and structure coated therewith
JPH01297462A (en) * 1988-05-25 1989-11-30 Tech Res & Dev Inst Of Japan Def Agency Coloring composition for camouflaging and camouflaged colored material
JPH02180631A (en) * 1988-11-17 1990-07-13 Minnesota Mining & Mfg Co <3M> Hollow ceramic microsphere produced by sol-gel process and manufacture thereof
JPH02216102A (en) * 1989-02-17 1990-08-29 Dainichiseika Color & Chem Mfg Co Ltd Coloring composition for color filter, production of color filter and color filter
JPH0345703A (en) * 1989-07-14 1991-02-27 Dainichiseika Color & Chem Mfg Co Ltd Artificial hair
JPH03266685A (en) * 1990-03-16 1991-11-27 Dainichiseika Color & Chem Mfg Co Ltd Method and material for recording
JPH04173833A (en) * 1990-11-07 1992-06-22 Natl Space Dev Agency Japan<Nasda> Light and heat insulating resin composition
JPH04246478A (en) * 1991-01-31 1992-09-02 Nippon Paint Co Ltd Article coated in deep color
JPH05293434A (en) * 1992-04-15 1993-11-09 Nippon Steel Chem Co Ltd Car body and part
JPH06100796A (en) * 1992-09-22 1994-04-12 Ito Sangyo:Yugen Coating material and heat-shutting, heat-insulating technique
JPH08127736A (en) * 1994-10-31 1996-05-21 Riboole:Kk Heat-insulating coating material
WO1997016493A1 (en) * 1995-11-01 1997-05-09 Herberts Gesellschaft mit beschränkter Haftung Agent for producing heat-reflecting coatings
JPH09241529A (en) * 1996-03-06 1997-09-16 Dainichiseika Color & Chem Mfg Co Ltd Particulate black composite-oxide pigment and production thereof
JPH1067947A (en) * 1996-08-29 1998-03-10 Dainichiseika Color & Chem Mfg Co Ltd Resin composition having protective abilities for temperature rise and heat accumulation by sunlight
JPH10282311A (en) * 1997-04-11 1998-10-23 Dainichiseika Color & Chem Mfg Co Ltd Black matrix coloring composition, manufacture of black matrix and part with shading black matrix
JPH1158582A (en) * 1997-08-27 1999-03-02 Soko Seiren Kk Light and heat shielding coating material
JPH1180624A (en) * 1997-09-09 1999-03-26 Nisshin Steel Co Ltd Heat reflecting coating composition and coated product
JPH11130966A (en) * 1997-08-28 1999-05-18 Mitsui Mining & Smelting Co Ltd Heat-ray-nonabsorbent coloring composition containing metal semiconductor powder and molded article
JPH11302549A (en) * 1998-04-22 1999-11-02 Origin Electric Co Ltd Infrared-reflective composition and infrared reflector
JP2000072990A (en) * 1998-08-31 2000-03-07 Nippon Paint Co Ltd Heat-ray-intercepting coating material
JP2000080319A (en) * 1998-04-17 2000-03-21 Clariant Gmbh Infrared reflecting colorant
JP2000126678A (en) * 1998-10-27 2000-05-09 Nagashima Tokushu Toryo Kk Coated metallic sheet coated with heat shieldable coating material

Patent Citations (46)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3577379A (en) * 1969-03-11 1971-05-04 Us Army Dark colored coatings of high solar heat reflectance
US3700397A (en) * 1969-05-06 1972-10-24 Us Army Camouflaged article and method of producing same
JPS4848529A (en) * 1971-10-25 1973-07-10
JPS5430221A (en) * 1977-08-11 1979-03-06 Dainichi Seika Kogyo Kk Preparation of azo pigments
JPS54141821A (en) * 1978-04-27 1979-11-05 Dainichi Seika Kogyo Kk Azo pigment
JPS54150498A (en) * 1978-05-18 1979-11-26 Mitsui Petrochem Ind Ltd Epoxy resin composition
JPS5527272A (en) * 1978-08-19 1980-02-27 Jirou Takei Method of producing heat shielding metal face plate
JPS56109257A (en) * 1980-01-22 1981-08-29 Aburamobuna Shiyuterun Maria Heat reflective enamel
JPS5649757A (en) * 1980-08-01 1981-05-06 Dainichi Seika Kogyo Kk Azo pigment
JPS5655456A (en) * 1980-08-01 1981-05-16 Dainichi Seika Kogyo Kk Azo pigment
JPS58167642A (en) * 1982-03-08 1983-10-03 ザ・ビー・エフ・グッドリッチ・カンパニー Infrared ray reflective vinyl polymer composition
JPS58174446A (en) * 1982-04-07 1983-10-13 Dainichi Seika Kogyo Kk Azo pigment and its preparation
JPS60149666A (en) * 1984-01-17 1985-08-07 Dainichi Seika Kogyo Kk Azo pigment and production thereof
JPS6230202A (en) * 1985-08-01 1987-02-09 Dainichi Color & Chem Mfg Co Ltd Infrared reflective material
JPS6268858A (en) * 1985-09-20 1987-03-28 Dainichi Color & Chem Mfg Co Ltd Infrared-reflective material
JPS6268855A (en) * 1985-09-20 1987-03-28 Dainichi Color & Chem Mfg Co Ltd Infrared-reflective material
US4624710A (en) * 1985-09-30 1986-11-25 Harshaw/Filtrol Partnership Pigment consisting of a mixture of chromium oxide and iron oxide useful in high infra red reflectance gray vinyl composition
JPS6279257A (en) * 1985-10-01 1987-04-11 Mitsubishi Heavy Ind Ltd Lightweight, heat insulating coating material
JPS62138857A (en) * 1985-12-12 1987-06-22 Dainichi Color & Chem Mfg Co Ltd Coloring composition for recording image
JPS6232149A (en) * 1986-03-07 1987-02-12 Dainichi Color & Chem Mfg Co Ltd Azo compound and colored composition
JPS6391283A (en) * 1986-10-07 1988-04-21 Dainichi Color & Chem Mfg Co Ltd Printed matter and production thereof
JPS63223076A (en) * 1987-03-13 1988-09-16 Seiko Epson Corp Titanium oxide-containing coating compound and coating film
JPS63275682A (en) * 1987-05-07 1988-11-14 Seiko Epson Corp Coating composition containing titanium oxide
JPH01126376A (en) * 1987-11-12 1989-05-18 Nippon Steel Chem Co Ltd Solar-heat shielding coated structure
JPH01263163A (en) * 1988-04-15 1989-10-19 Nippon Steel Chem Co Ltd Solar heat-shielding coating composition and structure coated therewith
JPH01297462A (en) * 1988-05-25 1989-11-30 Tech Res & Dev Inst Of Japan Def Agency Coloring composition for camouflaging and camouflaged colored material
JPH02180631A (en) * 1988-11-17 1990-07-13 Minnesota Mining & Mfg Co <3M> Hollow ceramic microsphere produced by sol-gel process and manufacture thereof
JPH02216102A (en) * 1989-02-17 1990-08-29 Dainichiseika Color & Chem Mfg Co Ltd Coloring composition for color filter, production of color filter and color filter
JPH0345703A (en) * 1989-07-14 1991-02-27 Dainichiseika Color & Chem Mfg Co Ltd Artificial hair
JPH03266685A (en) * 1990-03-16 1991-11-27 Dainichiseika Color & Chem Mfg Co Ltd Method and material for recording
JPH04173833A (en) * 1990-11-07 1992-06-22 Natl Space Dev Agency Japan<Nasda> Light and heat insulating resin composition
JPH04246478A (en) * 1991-01-31 1992-09-02 Nippon Paint Co Ltd Article coated in deep color
JPH05293434A (en) * 1992-04-15 1993-11-09 Nippon Steel Chem Co Ltd Car body and part
JPH06100796A (en) * 1992-09-22 1994-04-12 Ito Sangyo:Yugen Coating material and heat-shutting, heat-insulating technique
JPH08127736A (en) * 1994-10-31 1996-05-21 Riboole:Kk Heat-insulating coating material
WO1997016493A1 (en) * 1995-11-01 1997-05-09 Herberts Gesellschaft mit beschränkter Haftung Agent for producing heat-reflecting coatings
JPH09241529A (en) * 1996-03-06 1997-09-16 Dainichiseika Color & Chem Mfg Co Ltd Particulate black composite-oxide pigment and production thereof
JPH1067947A (en) * 1996-08-29 1998-03-10 Dainichiseika Color & Chem Mfg Co Ltd Resin composition having protective abilities for temperature rise and heat accumulation by sunlight
JPH10282311A (en) * 1997-04-11 1998-10-23 Dainichiseika Color & Chem Mfg Co Ltd Black matrix coloring composition, manufacture of black matrix and part with shading black matrix
JPH1158582A (en) * 1997-08-27 1999-03-02 Soko Seiren Kk Light and heat shielding coating material
JPH11130966A (en) * 1997-08-28 1999-05-18 Mitsui Mining & Smelting Co Ltd Heat-ray-nonabsorbent coloring composition containing metal semiconductor powder and molded article
JPH1180624A (en) * 1997-09-09 1999-03-26 Nisshin Steel Co Ltd Heat reflecting coating composition and coated product
JP2000080319A (en) * 1998-04-17 2000-03-21 Clariant Gmbh Infrared reflecting colorant
JPH11302549A (en) * 1998-04-22 1999-11-02 Origin Electric Co Ltd Infrared-reflective composition and infrared reflector
JP2000072990A (en) * 1998-08-31 2000-03-07 Nippon Paint Co Ltd Heat-ray-intercepting coating material
JP2000126678A (en) * 1998-10-27 2000-05-09 Nagashima Tokushu Toryo Kk Coated metallic sheet coated with heat shieldable coating material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
社団法人塗料工業会塗料原料便覧作成委員会編 , 塗料原料便覧第6版, JPN6008056659, 30 August 1993 (1993-08-30), JP, pages 188 - 190, ISSN: 0001175134 *

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006015193A (en) * 2004-06-30 2006-01-19 Dainippon Ink & Chem Inc Coating film forming method
WO2009125478A1 (en) * 2008-04-09 2009-10-15 Sci-Paint Japan株式会社 Thermal insulation coating material
JP4855477B2 (en) * 2008-04-09 2012-01-18 Sci−Paint Japan株式会社 Thermal barrier coating material
JP2009286862A (en) * 2008-05-28 2009-12-10 Nippon Paint Co Ltd Heat-insulating coating material composition, method for forming heat-insulating coating film using the same and heat-insulating coating film
WO2010106890A1 (en) 2009-03-17 2010-09-23 東洋アルミニウム株式会社 Method for reflecting infrared light
CN101531863B (en) * 2009-04-21 2011-09-28 厦门双瑞船舶涂料有限公司 A low solar absorbing energy-saving type neutral gray hull finish coat
CN104250513A (en) * 2014-09-25 2014-12-31 南京理工大学 Yellow-brown near-infrared reflection type thermal-insulating coating and preparation method thereof
CN104250514A (en) * 2014-09-25 2014-12-31 南京理工大学 Deep brown near-infrared reflection type heat insulation coating and preparation method thereof
CN104250513B (en) * 2014-09-25 2016-07-06 南京理工大学 A kind of yellowish-brown near-infrared reflection type insulating moulding coating and preparation method thereof
CN105368180A (en) * 2015-11-23 2016-03-02 安徽酉阳防水科技有限公司 Building insulation exterior wall heat-insulation paint having strong crack-resistance performance

Similar Documents

Publication Publication Date Title
JP3794837B2 (en) Thermal barrier paint and coating method thereof
JP4138129B2 (en) Solar heat shielding paint
US5962143A (en) Coating composition for producing heat radiation-reflecting coatings
JP6026938B2 (en) Thermal barrier matte water-based coating composition and thermal barrier matte coating film forming method
JP3468698B2 (en) Heat shield
US20050215685A1 (en) Infrared reflective wall paint
JPH04255769A (en) Black coating composition and coated structure for shielding solar heat
KR960014751B1 (en) Solar heat covering paint composition and coated structure
KR20190090957A (en) 2-coat-type aqueous heat-shielding and water-resistant paint for rooftop or roof, method for forming a heat-shielding and water-resistant coating with two layers structure using the same, and a heat-shielding and water-resistant coating with two layers structure thereby
JP2007016558A (en) Construction material board and manufacturing method therefor
WO1989004351A1 (en) Solar heat insulating paint composition and structures coated with said composition
US6734224B2 (en) Heat radiation shield coating composition
JP2011079908A (en) Coating composition and construction method
JPH01121371A (en) Coating composition for shielding solar heat
JP5537759B2 (en) Heat-reflective coating composition and coated article
JP2004027241A (en) Thermal insulation coating and its coating method
JP2000126678A (en) Coated metallic sheet coated with heat shieldable coating material
JP5113638B2 (en) Metallic matte design coating Metal plate coating method
JP2001089871A (en) Coated metallic sheet high in solar heat reflectibility
JP4512935B2 (en) Thermal insulation (heat insulation) method and thermal insulation material
JP2002320912A (en) Applying method for thermal-insulative color coating material and siding material
JP2003166305A (en) Heat-insulative aluminum curtain wall
JP6010315B2 (en) Matting multilayer film forming method for ceramics building materials
JP5461139B2 (en) Coating composition
JPH08302239A (en) Transparent coating

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20051026

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20081111

A711 Notification of change in applicant

Free format text: JAPANESE INTERMEDIATE CODE: A711

Effective date: 20081111

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A821

Effective date: 20081111

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20090313