JPH0643267B2 - Infrared radiation coating - Google Patents

Infrared radiation coating

Info

Publication number
JPH0643267B2
JPH0643267B2 JP61132324A JP13232486A JPH0643267B2 JP H0643267 B2 JPH0643267 B2 JP H0643267B2 JP 61132324 A JP61132324 A JP 61132324A JP 13232486 A JP13232486 A JP 13232486A JP H0643267 B2 JPH0643267 B2 JP H0643267B2
Authority
JP
Japan
Prior art keywords
coating
base material
infrared radiation
polytitanocarbosilane
film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
JP61132324A
Other languages
Japanese (ja)
Other versions
JPS62288152A (en
Inventor
正雄 牧
康典 金子
明雄 福田
守 礒谷
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 JP61132324A priority Critical patent/JPH0643267B2/en
Publication of JPS62288152A publication Critical patent/JPS62288152A/en
Publication of JPH0643267B2 publication Critical patent/JPH0643267B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 産業上の利用分野 本発明は、暖房、調理等で輻射加熱を行う赤外線加熱の
分野で、高効率の赤外線輻射体を形成するため、金属、
セラミックなどの加熱体表面に適用する被膜に関するも
のである。とくに、ステンレス等の耐熱性金属基材を対
象としている。
TECHNICAL FIELD The present invention is in the field of infrared heating for performing radiant heating in heating, cooking, etc., in order to form a highly efficient infrared radiant body, metal,
The present invention relates to a coating applied to the surface of a heating body such as ceramics. In particular, it is targeted at heat resistant metal base materials such as stainless steel.

従来の技術 従来の赤外線輻射コーティングとしては、アルミナ、チ
タニア、ジルコニアなどの酸化物、あるいは化合物を溶
射にて直接基材上に被覆形成したり、焼結させたりする
もの。更には、ガラスフリット等のバインダー中に分散
させ、ホウロウ被覆を形成したりするものが知られてい
る。
2. Description of the Related Art Conventional infrared radiation coating is a method in which oxides or compounds such as alumina, titania, zirconia, etc. are directly formed on the substrate by thermal spraying or sintered. Further, it is known to form a enamel coating by dispersing it in a binder such as glass frit.

溶射法の場合にはその被膜形成工程が非常に複雑である
上に膜厚が厚いため、基材との膨脹率の差を吸収させる
観点から、使用材料が制約される。また、形成した被膜
はポーラスで耐食性が劣っていた。
In the case of the thermal spraying method, the coating film forming process is very complicated and the film thickness is large, so that the material to be used is restricted from the viewpoint of absorbing the difference in expansion coefficient from the base material. In addition, the formed coating was porous and inferior in corrosion resistance.

焼結法の場合には、1300〜1400℃程度の加熱が
必要なため、基材として特殊セラミックを用いる必要が
あった。
In the case of the sintering method, since heating at about 1300 to 1400 ° C. is required, it is necessary to use a special ceramic as a base material.

また、ホウロウ系の場合には、膜厚が100μm以上と
厚いため、熱膨脹係数が合わず基材との密着が悪かった
り、500℃以上に加熱すると被膜が流動性を示したり
することから、500℃以上の高温下では適用できない
欠点があった。
Further, in the case of the enamel type, since the film thickness is as thick as 100 μm or more, the coefficient of thermal expansion does not match and the adhesion with the substrate is poor, or the coating film exhibits fluidity when heated to 500 ° C. or more. There was a drawback that it could not be applied at high temperatures above ℃.

更に、シリカ等をバインダーとする耐熱塗装をステンレ
ス等の耐食性基材上に形成するコーティングが知られて
いる。これ等の耐熱塗装の場合には、耐ヒートショック
性などの特性を有利にするために、塗膜をポーラスに形
成する必要があるが、耐湿、耐食性の厳しい環境で用い
る場合、隙間腐食を起こし、耐食性に難点があった。
Further, a coating is known in which a heat resistant coating using silica or the like as a binder is formed on a corrosion resistant substrate such as stainless steel. In the case of heat resistant coatings such as these, it is necessary to form a coating film in order to make properties such as heat shock resistance advantageous, but when used in an environment with severe humidity and corrosion resistance, crevice corrosion will occur. There was a problem in corrosion resistance.

発明が解決しようとする問題点 本発明は、このような従来の欠点を解消するもので、1
0〜50μmの薄膜の形成によって、赤外線放射率が0.
8以上の赤外線高輻射被膜を提供するものである。金属
面への被膜の形成が、通常の有機塗装と同様の方法にて
可能で、500℃までの加熱面で、とくに苛酷な腐食環
境に対して、優れた接着信頼性を有する被膜を提供する
ことも、本発明の狙いである。従来、この種の技術は、
ほとんど知られていなかった。
DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention The present invention solves the above-mentioned conventional drawbacks.
By forming a thin film of 0 to 50 μm, the infrared emissivity is 0.
It provides an infrared high radiation coating of 8 or more. A film can be formed on a metal surface by the same method as that of ordinary organic coating, and a film having excellent adhesion reliability is provided on a surface heated up to 500 ° C, particularly in a severe corrosive environment. This is also the aim of the present invention. Traditionally, this kind of technology
Little was known.

問題点を解決するための手段 本発明は前記課題を解決するために、表面粗さ0.4μm
以上の基板上に、ポリチタノカルボシランを結合剤とし
て、フッ素樹脂を結合剤に対して、5〜15重量部含有
し、その他充填剤、顔料の硬化体よりなり、被膜中の金
属含有率が2wt%以下である被膜を形成して用いる。
Means for Solving the Problems In order to solve the above problems, the present invention has a surface roughness of 0.4 μm.
On the above substrate, polytitanocarbosilane was used as a binder, fluororesin was contained in an amount of 5 to 15 parts by weight with respect to the binder, and other fillers and a cured product of pigment were used. Is used to form a coating having a content of 2 wt% or less.

ポリチタノカルボシランを溶剤に溶解した状態で、その
他の添加物を前記結合剤中に分散させ、塗料化したもの
を用いて、対象とする表面粗さ0.3μm以上の基材上に
塗布・焼成した後の硬化体として、赤外線輻射被膜を得
る。
In a state where polytitanocarbosilane is dissolved in a solvent, other additives are dispersed in the binder, and a paint is used to apply it to a target substrate having a surface roughness of 0.3 μm or more. An infrared radiation coating is obtained as a cured product after firing.

作用 ポリチタノカルボシランは、ジメチルジクロロシランの
脱塩素重縮合反応により合成されるポリジメチルシラン
に、ジフェニルジクロロシランとホウ酸の重縮合により
得られるポリボロジフェニルシロキサンと呼ばれる半無
機ポリマーと、チタン化合物とを加熱重縮合させて得ら
れる。
Action Polytitanocarbosilane is a polydimethylsilane synthesized by dechlorination polycondensation reaction of dimethyldichlorosilane, a semi-inorganic polymer called polyborodiphenylsiloxane obtained by polycondensation of diphenyldichlorosilane and boric acid, and titanium. It is obtained by heat polycondensation with a compound.

ポリチタノカルボシランは主としてカルボシラン骨格か
らなるポリカルボシラン部分がチタン化合物によって架
橋重合された有機金属架橋重合体であり、 のような基本構造単位から成っている。
Polytitanocarbosilane is an organometallic crosslinked polymer in which a polycarbosilane moiety mainly composed of a carbosilane skeleton is crosslinked and polymerized with a titanium compound, It is made up of basic structural units such as.

このポリチタノカルボシランは有機溶媒に容易に溶解す
るため、溶解させた状態で用いる。ポリチタノカルボシ
ランは分子量5,000〜50,000の範囲のものの
適用が望ましい。
Since this polytitanocarbosilane is easily dissolved in an organic solvent, it is used in a dissolved state. It is desirable to use polytitanocarbosilane having a molecular weight of 5,000 to 50,000.

フッ素樹脂は分子量1,000〜8,000程度で粒径
が0.1〜1μm程度の微粉末を用いる。
As the fluororesin, fine powder having a molecular weight of about 1,000 to 8,000 and a particle size of about 0.1 to 1 μm is used.

その他、赤外線放射率を高めるため、充填剤、顔料を配
合する。これ等の充填剤、顔料としては、ジルコニウ
ム、ケイ素、アルミニウム、チタンの群から選定した1
種以上の元素の酸化物、炭化物、窒化物および、鉄、マ
ンガン、銅、ニッケル、コバルトの群から選定した少な
くとも1種の元素の酸化物、複合酸化物などを主成分と
して用いても良い。前者は白色化合物であり、後者は着
色化合物である。前者の白色化合物は、6μm以上の長
波長の赤外線領域に高い吸収係数をもっている。後者の
遷移元素酸化物は黒色化合物で、逆に6μm以下の短波
長側で高い吸収係数をもつ。そこで、両者を適当に配合
することで、赤外線の全波長域にわたって、高い赤外線
輻射率をもった被膜が得られる。これ等の充填剤、顔料
の粒径としては、0.05〜1μmの範囲のものを用いるの
が望ましい。充填剤のポリチタノカルボシランに対する
配合比は重量比で1/2〜3/2の範囲、顔料のポリチ
タノカルボシランに対する配合比は重量比で1/2〜1
/1の範囲を用いるのが望ましい。
In addition, a filler and a pigment are added to increase the infrared emissivity. These fillers and pigments are selected from the group consisting of zirconium, silicon, aluminum and titanium 1
As the main component, oxides, carbides, and nitrides of one or more elements, and oxides and complex oxides of at least one element selected from the group of iron, manganese, copper, nickel, and cobalt may be used. The former is a white compound and the latter is a colored compound. The former white compound has a high absorption coefficient in the infrared region having a long wavelength of 6 μm or more. The latter transition element oxide is a black compound, and conversely has a high absorption coefficient on the short wavelength side of 6 μm or less. Therefore, by appropriately mixing both, a coating having a high infrared emissivity over the entire infrared wavelength range can be obtained. The particle size of these fillers and pigments is preferably in the range of 0.05 to 1 μm. The compounding ratio of the filler to the polytitanocarbosilane is in the range of 1/2 to 3/2 by weight, and the compounding ratio of the pigment to the polytitanocarbosilane is in the range of 1/2 to 1 by weight.
It is desirable to use the range of / 1.

実施例 以下、本発明の実施例を添付図面に基づいて説明する。Embodiment An embodiment of the present invention will be described below with reference to the accompanying drawings.

第1図は本発明の被膜の概念図である。表面粗さ0.3以
上の基板上に、ポリチタノカルボシラン2を結合剤とし
て、この中に、フッ素樹脂3、充填剤4、顔料5を含有
する被膜を形成する。被膜は、充填剤4と顔料5の含有
により、高い赤外線放射率を示す。この種の被膜が耐熱
性をもつためには、被膜がポーラスであることが必要
で、これが基材との熱膨脹率の差を吸収し、ヒートショ
ックに耐え得る被膜となるが、このため、逆に耐湿性、
耐食性などが低下し、被膜のピンホールを介して基材が
腐食する。とくにステンレスを基材として用いる場合に
は、隙間腐食の進行が著しい。
FIG. 1 is a conceptual diagram of the coating film of the present invention. On a substrate having a surface roughness of 0.3 or more, a coating containing fluororesin 3, filler 4, and pigment 5 is formed by using polytitanocarbosilane 2 as a binder. The coating shows a high infrared emissivity due to the inclusion of the filler 4 and the pigment 5. In order for this type of coating to have heat resistance, it is necessary that the coating be porous, which absorbs the difference in the coefficient of thermal expansion from the base material and can withstand heat shock. To moisture resistance,
Corrosion resistance decreases, and the base material corrodes through the pinholes in the coating. Especially, when stainless steel is used as the base material, the progress of crevice corrosion is remarkable.

本発明の場合には、フッ素樹脂3を被膜内に含有してい
るため、被膜が揆水性を有するので優れた耐食性をも
つ。
In the case of the present invention, since the fluororesin 3 is contained in the coating film, the coating film has water repellent property and thus has excellent corrosion resistance.

通常、この種の塗料を調合する場合には、塗料分散機を
用いて塗料を調合する。通常、スチールボールなどのメ
ディア中で塗料を攪拌して塗料を調合するが、分散時に
メデイアが磨耗して、塗料中に混入する。ステンレスを
基材として用いる場合、金属系メディアが被膜中への混
入すると、この金属が耐食性環境で腐食し、この結果生
じた金属イオンがステンレス基材を還元し、ステンレス
基材の著しい腐食を起こすことが分った。金属系メディ
アに起因する被膜中への金属の混入量は、2wt%以下の
場合に、基材の腐食の影響が認められないことを確認し
た。
Usually, when preparing this kind of paint, the paint is prepared using a paint disperser. Usually, the paint is prepared by stirring the paint in a medium such as a steel ball, but the media wears during dispersion and mixes into the paint. When stainless steel is used as the base material, if metal-based media is mixed in the coating, the metal corrodes in a corrosion resistant environment, and the resulting metal ions reduce the stainless steel base material, causing significant corrosion of the stainless steel base material. I found out. It was confirmed that the influence of corrosion of the base material was not observed when the amount of metal mixed in the coating film due to the metal-based medium was 2 wt% or less.

ポリチタノカルボシランは、宇部興産株式会社の「チラ
ノコート」を用いた。
As the polytitanocarbosilane, "Tyrannocoat" manufactured by Ube Industries, Ltd. was used.

前記チラノコート100重量部に対して、第1表の配合
にて塗料を調合した。第1表の塗料を20μmの膜厚に
て、表面粗さの異なった各種基材上に塗布し300℃に
て30分焼成したものについて、200時間の連続の塩
水噴霧試験後、セロテープ剥離試験を実施した結果を表
2に示す。尚ステンレスは基材として、SUS−304
を用いた。表面仕上の異なる2種類の基材について試験
した。表面粗度は、中心線表面粗さ(ra)で表わした。
A coating material was prepared according to the composition shown in Table 1 with respect to 100 parts by weight of the Tyranno coat. The coating material of Table 1 having a film thickness of 20 μm was coated on various substrates having different surface roughness and baked at 300 ° C. for 30 minutes. After continuous salt spray test for 200 hours, cellophane tape peeling test was performed. The results of carrying out are shown in Table 2. In addition, stainless steel is used as a base material for SUS-304.
Was used. Two types of substrates having different surface finishes were tested. The surface roughness is expressed by the center line surface roughness (ra).

次に、表面粗さの異なった4種類の試料について、P−
2の塗料で同様の試験を実施した。試料の表面粗さは、
0.22、0.28、0.44、0.47であった。この結果は、前2者が
剥離であったのに対して、後2者はほとんど剥離は認め
られなかった。基材の種類をSUS−321に変えて試
験した所、錆の発生は少なかったが、同様の傾向が認め
られた。以上から、当組成の塗料に関しては基材の表面
粗さ0.4μm以上が有効と考えられる。更にフッ素樹脂
の配合に関しては、5重量部から有効であるが、20重
量部を越えると基材との密着性が低下してくるものと考
えられる。尚、これ等の被膜はいずれも、優れた赤外線
輻射性能を示し、赤外線放射率は、0.8以上であった。
Next, for four types of samples with different surface roughness, P-
A similar test was performed with the two paints. The surface roughness of the sample is
It was 0.22, 0.28, 0.44 and 0.47. As a result, peeling was observed in the former two cases, whereas peeling was hardly observed in the latter two cases. When the type of the base material was changed to SUS-321 and tested, the occurrence of rust was small, but the same tendency was observed. From the above, it is considered that the surface roughness of the base material of 0.4 μm or more is effective for the coating composition of this composition. Further, regarding the blending of the fluororesin, it is effective from 5 parts by weight, but if it exceeds 20 parts by weight, it is considered that the adhesion to the base material is deteriorated. All of these coatings showed excellent infrared radiation performance, and the infrared emissivity was 0.8 or more.

本被膜の膜厚については、10μm以下となると、輻射
率も低下し、耐食性も低下する。また50μmを越える
と、被膜はヒートショックに対して弱くなる。
When the film thickness of the present coating is 10 μm or less, the emissivity decreases and the corrosion resistance also decreases. When it exceeds 50 μm, the coating becomes weak against heat shock.

本被膜は鉛筆硬度7H以上の硬い被膜で、500℃の加熱
環境下でも、十分優れた密着信頼性を保持している。
This coating is a hard coating with a pencil hardness of 7H or more, and has sufficiently excellent adhesion reliability even under a heating environment of 500 ° C.

とくに、耐ヒートショック性に優れ、500℃から水中
に冷却しても、被膜には剥離、割れなどの異常は認めら
れなかった。
In particular, it was excellent in heat shock resistance, and even when it was cooled from 500 ° C. to water, no abnormality such as peeling or cracking was observed in the coating.

発明の効果 以上のように本発明の効果は、 (1)ステンレスなどの耐熱金属上に形成した耐熱被膜で
あるが、激しい腐食環境下でも極めて優れた耐食性を有
する被膜が得られる。
Effects of the Invention As described above, the effects of the present invention are (1) a heat resistant coating formed on a heat resistant metal such as stainless steel, but a coating having extremely excellent corrosion resistance even in a severe corrosive environment can be obtained.

(2)10〜50μmと薄膜であるにも拘らず、赤外線輻
射率0.8以上の耐熱性の優れた輻射体が得られる。
(2) Although it is a thin film having a thickness of 10 to 50 μm, a radiator having an infrared emissivity of 0.8 or more and excellent heat resistance can be obtained.

(3)スプレー法で塗布可能であり、静電塗装が可能であ
る。通常の有機塗料と同じ脱脂などの工程で簡単に被膜
が形成でき、生産性に優れているため安価である。
(3) It can be applied by spraying, and electrostatic coating is possible. A film can be easily formed in the same degreasing process as that for ordinary organic paints, and it is inexpensive because it has excellent productivity.

(4)最終300℃の加熱で被膜が形成できるため、多く
の耐熱金属上への適用が可能である。
(4) Since the coating can be formed by heating at 300 ° C. at the end, it can be applied to many heat-resistant metals.

(5)スプレー法で塗布できるため、金網状金属など複雑
な基材への適用が可能である。
(5) Since it can be applied by a spray method, it can be applied to complicated base materials such as wire mesh metal.

(6)薄膜のため、極めて密着性が良好で、とくに耐ヒー
トショックに強く、高信頼性の被膜が得られる。
(6) Since it is a thin film, it has extremely good adhesion and is particularly resistant to heat shock, and a highly reliable film can be obtained.

などの効果を有する。And so on.

【図面の簡単な説明】[Brief description of drawings]

図は本発明の一実施例の赤外線輻射被膜の要部断面図で
ある。 1……表面粗さ0.3以上の基板、2……ポリチタノカル
ボシラン、3……フッ素樹脂、4……充填剤、5……顔
料。
FIG. 1 is a sectional view of a main part of an infrared radiation coating according to an embodiment of the present invention. 1 ... Substrate with surface roughness of 0.3 or more, 2 ... Polytitanocarbosilane, 3 ... Fluorine resin, 4 ... Filler, 5 ... Pigment.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 礒谷 守 大阪府門真市大字門真1006番地 松下電器 産業株式会社内 (56)参考文献 特開 昭62−167271(JP,A) 特開 昭60−27669(JP,A) ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Mamoru Isotani 1006 Kadoma, Kadoma City, Osaka Prefecture Matsushita Electric Industrial Co., Ltd. (56) Reference JP-A-62-167271 (JP, A) JP-A-60- 27669 (JP, A)

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】表面粗さ0.4μm以上の基板上に、ポリチ
タノカルボシランを結合剤として、フッ素樹脂を結合剤
に対して、5〜15重量部含有し、その他充填剤、顔料
の硬化体よりなり、被膜中の金属含有率が2wt%以下で
ある赤外線輻射被膜。
1. A substrate having a surface roughness of 0.4 μm or more, containing 5 to 15 parts by weight of a fluororesin as a binder and a fluororesin as a binder, and curing other fillers and pigments. An infrared radiation coating consisting of a body and having a metal content of 2 wt% or less.
JP61132324A 1986-06-06 1986-06-06 Infrared radiation coating Expired - Lifetime JPH0643267B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61132324A JPH0643267B2 (en) 1986-06-06 1986-06-06 Infrared radiation coating

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61132324A JPH0643267B2 (en) 1986-06-06 1986-06-06 Infrared radiation coating

Publications (2)

Publication Number Publication Date
JPS62288152A JPS62288152A (en) 1987-12-15
JPH0643267B2 true JPH0643267B2 (en) 1994-06-08

Family

ID=15078653

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61132324A Expired - Lifetime JPH0643267B2 (en) 1986-06-06 1986-06-06 Infrared radiation coating

Country Status (1)

Country Link
JP (1) JPH0643267B2 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01142192U (en) * 1988-03-24 1989-09-28
JPH0249391A (en) * 1988-08-10 1990-02-19 Kurosaki Rokougiyou Kk Infrared ray generating heater using synthetic resin
JPH0229192U (en) * 1988-08-18 1990-02-26
JP2523271Y2 (en) * 1989-12-07 1997-01-22 シャープ株式会社 microwave
JP2559100Y2 (en) * 1995-09-20 1998-01-14 シャープ株式会社 microwave

Also Published As

Publication number Publication date
JPS62288152A (en) 1987-12-15

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