JP2833142B2 - Paint cured film and cooker having the same - Google Patents
Paint cured film and cooker having the sameInfo
- Publication number
- JP2833142B2 JP2833142B2 JP2097956A JP9795690A JP2833142B2 JP 2833142 B2 JP2833142 B2 JP 2833142B2 JP 2097956 A JP2097956 A JP 2097956A JP 9795690 A JP9795690 A JP 9795690A JP 2833142 B2 JP2833142 B2 JP 2833142B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- paint
- cooker
- copper
- cured 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 - Fee Related
Links
- 239000003973 paint Substances 0.000 title claims description 14
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims description 36
- 229960004643 cupric oxide Drugs 0.000 claims description 18
- 239000000463 material Substances 0.000 claims description 11
- 229910052751 metal Inorganic materials 0.000 claims description 10
- 239000002184 metal Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052796 boron Inorganic materials 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 239000010703 silicon Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 3
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 3
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 claims description 2
- 239000005750 Copper hydroxide Substances 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- 229940116318 copper carbonate Drugs 0.000 claims description 2
- 229910001956 copper hydroxide Inorganic materials 0.000 claims description 2
- 239000010936 titanium Substances 0.000 claims description 2
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 239000011248 coating agent Substances 0.000 description 21
- 238000000576 coating method Methods 0.000 description 21
- 238000010411 cooking Methods 0.000 description 17
- 239000000835 fiber Substances 0.000 description 15
- 230000003197 catalytic effect Effects 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 239000003921 oil Substances 0.000 description 9
- 238000000354 decomposition reaction Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 240000008415 Lactuca sativa Species 0.000 description 3
- 235000012045 salad Nutrition 0.000 description 3
- 241001149724 Cololabis adocetus Species 0.000 description 2
- 239000005749 Copper compound Substances 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 150000001880 copper compounds Chemical class 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000011273 tar residue Substances 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 229910021536 Zeolite Inorganic materials 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002313 adhesive film Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-UHFFFAOYSA-N 0.000 description 1
- AEJIMXVJZFYIHN-UHFFFAOYSA-N copper;dihydrate Chemical compound O.O.[Cu] AEJIMXVJZFYIHN-UHFFFAOYSA-N 0.000 description 1
- KRFJLUBVMFXRPN-UHFFFAOYSA-N cuprous oxide Chemical compound [O-2].[Cu+].[Cu+] KRFJLUBVMFXRPN-UHFFFAOYSA-N 0.000 description 1
- 229940112669 cuprous oxide Drugs 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 229910000314 transition metal oxide Inorganic materials 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
- Catalysts (AREA)
- Paints Or Removers (AREA)
- Cookers (AREA)
Description
【発明の詳細な説明】 産業上の利用分野 本発明は、家庭用、業務用等の調理器から発生する汚
れを浄化する塗料硬化被膜およびそれを有する調理器に
関する。Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cured paint film for purifying stains generated from cooking appliances for home use, business use, and the like, and a cooking appliance having the same.
従来の技術 従来、調理器から発生する汚れを浄化する方式として
は、主に3方式があった、第1は、調理室内温度を450
〜500℃に加熱して汚れを熱分解する方式、第2は、調
理室壁面に触媒作用を有する遷移金属酸化物やゼオライ
ト等の触媒を含んだ被膜を形成し触媒作用により汚れを
分解する方式、第3は、調理室内壁に非粘着性膜を形成
し、付着した汚れを拭き取る方式である。2. Description of the Related Art Conventionally, there have been mainly three methods for purifying dirt generated from a cooking device.
The second method is to decompose dirt by heating to ~ 500 ° C. The second method is to form a film containing a catalyst such as a transition metal oxide or zeolite having a catalytic action on the wall surface of the cooking chamber and decompose the dirt by catalytic action. Third, a non-adhesive film is formed on the inner wall of the cooking chamber, and the adhered dirt is wiped off.
発明が解決しようとする課題 しかしながら上記従来技術では、以下のような課題が
ある。Problems to be Solved by the Invention However, the above conventional technology has the following problems.
第1の熱分解方式では、長時間高温になるため電子部
品等の熱劣化や安全性が課題であり、第2の触媒作用に
よる分解方式は触媒が被膜中の結合剤に覆われてしまう
ために高い活性が得られず、汚れの分解が不完全になる
ことと、触媒の一部が反応中に還元されて劣化するとい
う課題があり、非粘着性被膜による方式については拭き
取るという手間と被膜の耐熱温度が低いという課題であ
る。In the first thermal decomposition method, a high temperature is applied for a long time, so that thermal degradation and safety of electronic components and the like are problems. In the second thermal decomposition method, the catalyst is covered by a binder in a coating film. However, high activity is not obtained, and the decomposition of dirt becomes incomplete, and there is a problem that part of the catalyst is reduced during the reaction and deteriorates. Is low in heat resistance.
本発明はこのような課題を解決し、触媒作用による汚
れを浄化する塗料硬化被膜およびそれを有する調理器の
提供を目的とする。An object of the present invention is to solve such problems and to provide a cured coating film for purifying dirt due to a catalytic action and a cooker having the same.
課題を解決するための手段 上記目的を達成するために本発明は、シリコン、ボロ
ン、チタンおよび酸素から構成されるポリボロチタノシ
ロキサンまたはシリコン、ボロンおよび酸素から構成さ
れるポリボロシロキサンと繊維状の無機物と、酸化第二
銅(CuO)、炭酸銅(CuCO3)、水酸化銅[Cu(OH)2]
および酢酸銅[Cu(OOCCH3)2]のうちの一種以上の銅
の化合物と、溶剤とを混合した塗料を焼成硬化して触媒
作用を有する多孔質な塗料硬化被膜とする。さらにこの
塗料硬化皮膜を金属多孔体表面に形成して壁面材とし、
その壁面材を調理室内に少なくとも一面有する調理器と
するものである。Means for Solving the Problems In order to achieve the above object, the present invention provides a polyborotitanosiloxane composed of silicon, boron, titanium and oxygen or a polyborosiloxane composed of silicon, boron and oxygen and a fibrous material. Inorganic substances, cupric oxide (CuO), copper carbonate (CuCO 3 ), copper hydroxide [Cu (OH) 2 ]
A mixture of one or more compounds of copper and copper acetate [Cu (OOCCH 3 ) 2 ] and a solvent is baked and cured to form a cured porous coating film having a catalytic action. Further, this paint cured film is formed on the surface of the porous metal body to form a wall material,
The cooking device has at least one wall material in the cooking chamber.
作用 上記手段により、ポリボロチタノシロキサンまたはポ
リボロシロキサンは結合剤で、それ自身、単独では焼成
硬化しても造膜が困難であるが、充填材を適量配合すれ
ば容易に造膜し、しかも多孔質な被膜になりやすい。特
に、繊維状の無機物は多孔性を増加させる。その理由
は、繊維が直線状のため被膜中において繊維同志がから
み合い、空隙を作りやすいためである。By the above-mentioned means, polyborotitanosiloxane or polyborosiloxane is a binder, and it is difficult to form a film by itself by sintering and curing. Moreover, it is easy to become a porous film. In particular, fibrous minerals increase porosity. The reason for this is that the fibers are straight, so that the fibers are entangled with each other in the coating, and voids are easily formed.
調理による代表的な汚れである油汚れを触媒作用によ
り分解するのは酸化反応であり、酸素の存在が重要であ
る。その酸素は空気中から供給されるもので、酸素をよ
り多くとり込むには多孔質被膜であることが望まれる。
したがって上記のようにして得られる被膜は好適であ
る。It is an oxidation reaction to decompose oil stains, which are typical stains due to cooking, by catalytic action, and the presence of oxygen is important. The oxygen is supplied from the air, and a porous coating is desired to take in more oxygen.
Therefore, the coating obtained as described above is suitable.
さらに、触媒として作用する酸化第二銅はその粉末に
油(例えばサラダ油)をしみこませ、空気中で加熱(約
300〜350℃)させると油を酸化分解するが、反応の前後
で構造の変化がない。マンガン、コバルトなどの他の繊
維金属酸化物は反応中に還元されやすく構造が変化し活
性が低下したり、構造変化しない場合でも活性が酸化第
二銅に比べて低く、他元素との複合化などで対還元性を
向上させるなどしないかぎりは触媒としては不敵であ
る。これに対して、酸化第二銅は触媒としての活性もあ
り、かつ仮に反応中に酸化第一銅へ還元されても空気中
で、300℃以上の場合にはすぐに酸化第二銅へ容易に再
酸化されるため劣化することがほとんどない。前記のよ
うに被膜は多孔質であるために酸化第二銅は酸素を容易
にとりこんで油を触媒的に酸化分解できるし、劣化防止
も可能である。In addition, cupric oxide, which acts as a catalyst, impregnates the powder with oil (eg, salad oil) and heats it in air (approximately
(300-350 ° C), the oil is oxidatively decomposed, but there is no structural change before and after the reaction. Other fiber metal oxides such as manganese and cobalt are easily reduced during the reaction, change their structure and decrease their activity, and even when there is no structural change, their activity is lower than that of cupric oxide, and they can be combined with other elements. Unless the reducibility is improved by such a method, the catalyst is invulnerable. On the other hand, cupric oxide has activity as a catalyst, and even if reduced to cuprous oxide during the reaction, it is easily converted to cupric oxide immediately in air at 300 ° C or higher. It is hardly deteriorated because it is reoxidized. As described above, since the coating is porous, cupric oxide can easily take in oxygen to catalytically oxidize and decompose oil and prevent deterioration.
また炭酸銅、水酸化銅、酢酸銅は焼成硬化中に分解し
て酸化第二銅となる一方、分解中に発生するガス(例え
ばCO2,H2O等)のために酸化第二銅の表面近傍に空隙を
つくりやすく、汚れの酸化分解に有利となる。Copper carbonate, copper hydroxide, and copper acetate are decomposed during sintering to form cupric oxide, while gases (eg, CO 2 , H 2 O) generated during decomposition decompose cupric oxide. Voids are easily formed near the surface, which is advantageous for oxidative decomposition of dirt.
次に、上記被膜を表面に形成した金属多孔体は、空隙
径が数100μmもあり、しかも連続孔であるため、従来
のような発泡による非連続孔の多孔体に比べて、油の吸
収拡散性や酸素拡散性がはるかに優れている。したがっ
て上記被膜の触媒作用を発揮するのに好適である。Next, since the porous metal body having the above-mentioned coating formed on the surface has a void diameter of several 100 μm and is a continuous hole, the absorption and diffusion of oil are larger than the conventional porous body having non-continuous pores due to foaming. The properties and oxygen diffusivity are much better. Therefore, it is suitable for exhibiting the catalytic action of the coating.
以上のような触媒作用を有する皮膜を金属多孔体の表
面に形成して壁面材とし、調理器の室内に配置すること
で、調理による汚れの触媒的な分解浄化が可能となる。By forming a film having a catalytic action as described above on the surface of the porous metal body to form a wall material and disposing the film in the cooking chamber, it becomes possible to catalytically decompose and purify dirt due to cooking.
実施例 以下、図面を用いて本発明の一実施例について説明す
る。Embodiment Hereinafter, an embodiment of the present invention will be described with reference to the drawings.
第1図は本発明による塗料硬化被膜とその塗料硬化被
膜を金属多孔体表面に形成した壁面材の断面図で、図に
おいて、1はポリボロチタノシロキサンの焼成硬化物、
2はシリカ・アルミナ繊維、3は酸化第二銅(CuO)、
4はアルミニウム長繊維である。FIG. 1 is a cross-sectional view of a cured coating film of the present invention and a wall material in which the cured coating film is formed on the surface of a porous metal body. In the drawing, 1 is a fired cured product of polyborotitanosiloxane;
2 is silica-alumina fiber, 3 is cupric oxide (CuO),
4 is an aluminum long fiber.
第2図は第1図に示した塗料硬化被膜を表面に形成し
たアルミニウム長繊維の壁面材5の拡大図で、第1図の
シリカ・アルミナ繊維2は直径が数μm、長さが数10〜
数100μm、アルミニウム長繊維4は直径が数10〜数100
μm、長さが数10mm、被膜の厚さは約20μm以下であ
る。FIG. 2 is an enlarged view of a wall material 5 made of an aluminum long fiber having a cured coating film shown in FIG. 1 formed on its surface. The silica-alumina fiber 2 shown in FIG. 1 has a diameter of several μm and a length of several tens. ~
Several hundred μm, diameter of aluminum long fiber 4 is several tens to several hundreds
μm, the length is several tens of mm, and the thickness of the coating is about 20 μm or less.
第3図(a)は第2図に示した壁面材(5)を調理室
内に設けた調理器(6)の斜視図で、第3図(b)は第
3図(a)におけるA部すなわち、壁面材(5)の拡大
正面図である。第3図(b)において、(7)はアルミ
ニウム長繊維を補強するために設けたアルミニウムエキ
スパンドメタルで、その表面にも塗料硬化被膜が形勢さ
れている。FIG. 3 (a) is a perspective view of a cooker (6) provided with the wall material (5) shown in FIG. 2 in a cooking chamber, and FIG. 3 (b) is a portion A in FIG. 3 (a). That is, it is an enlarged front view of the wall member (5). In FIG. 3 (b), (7) is an aluminum expanded metal provided to reinforce the aluminum long fiber, and a cured coating film is formed on the surface of the expanded metal.
以下、第1図、第2図、第3図に示した塗料硬化被膜
とそれを有する調理器の作用、効果について説明する。Hereinafter, the functions and effects of the paint cured film shown in FIGS. 1, 2 and 3 and the cooking device having the same will be described.
まず、塗料効果被膜について説明する。従来例として
無機リン酸塩と金属酸化物とからなる触媒作用を有する
被膜を用いた。下記の表に被膜中の触媒と、油の代表例
としてサラダ油を使ったときの分解浄化テストの結果を
示す。分解浄化テストにはアルミニウム長繊維積層体か
らなる多孔体表面に塗料硬化被膜を形成した100mm×100
mm×0.7mmのテストピースを使用し、テスト方法はサラ
ダ油約0.1gをテストピース上に5点に分けて滴下し、35
0℃の電気炉内で15分間放置を1サイクルとした。表中N
o.1〜7は本発明によるもので、ポリボロチタノシロキ
サン90重量部とシリカ・アルミナ繊維20重量部は共通で
あるので表には入れていない。また焼成は450℃、20分
で行った。表中、No.5〜7の銅化合物は焼成硬化により
CuOとなる。First, the paint effect coating will be described. As a conventional example, a film having a catalytic action composed of an inorganic phosphate and a metal oxide was used. The table below shows the catalyst in the coating and the results of the decomposition and purification tests using salad oil as a typical example of oil. In the decomposition and purification test, a paint cured film was formed on the surface of a porous body made of aluminum long fiber laminate, 100 mm × 100
Using a test piece of mm × 0.7mm, the test method is to drop about 0.1 g of salad oil into 5 points on the test piece,
One cycle was left in an electric furnace at 0 ° C. for 15 minutes. N in the table
Nos. 1 to 7 are according to the present invention and are not shown in the table because 90 parts by weight of polyborotitanosiloxane and 20 parts by weight of silica-alumina fiber are common. The firing was performed at 450 ° C. for 20 minutes. In the table, the copper compounds of Nos. 5 to 7 are cured by firing.
It becomes CuO.
上記表から明らかなように、CuOは多い方が好ましい
が、多すぎると被膜がもろくなり、60〜100重量部が望
ましい。表中、No.4は従来例に比べて優れており、CuO
の触媒作用と多孔質化されたテストピースの全体構成が
分解浄化に寄与していることが伺える。表中、No.4の被
膜をアルミニウム平板上に形成し分解浄化テストを行っ
たところ、1サイクルでタール残渣があったことも裏付
けとなる。 As is clear from the above table, it is preferable that the amount of CuO is large, but if it is too large, the coating becomes brittle, and 60 to 100 parts by weight is desirable. In the table, No. 4 is superior to the conventional example, and CuO
It can be seen that the catalytic action of the above and the overall structure of the porous test piece contributed to decomposition and purification. In the table, the coating No. 4 was formed on an aluminum flat plate and subjected to a decomposition and purification test, which proves that tar residues were found in one cycle.
次に、触媒のCuOであるが、それ自身が反応前後で構
造変化しないことはX線回折で確認され、例えば同じく
活性の高いMrO2はMr2O3へと還元され活性が低下した。Next, it was confirmed by X-ray diffraction that the catalyst itself, CuO, did not change its structure before and after the reaction. For example, similarly active MrO 2 was reduced to Mr 2 O 3 and the activity decreased.
なお、被膜中の繊維状無機物については、シリカ・ア
ルミナの他にジルコニア、炭化ケイ素、炭素も使用可能
で、これらの長繊維を短く粉砕して使うことができる。As the fibrous inorganic substance in the coating, zirconia, silicon carbide, and carbon can be used in addition to silica / alumina, and these long fibers can be used after being ground short.
また、金属多孔体については、アルミニウムの他にス
テンレスでもよく、これらはいずれも連続した多孔体で
ある。ステンレスの場合、繊維径はアルミニウムよりも
小さくなることもあるが、いずれも空隙率が50%以上あ
り触媒作用を発揮するのには好適である。The metal porous body may be stainless steel in addition to aluminum, and these are all continuous porous bodies. In the case of stainless steel, the fiber diameter may be smaller than that of aluminum, but all have a porosity of 50% or more and are suitable for exerting a catalytic action.
次に、第3図(a)に示した調理器で実際にサンマを
焼いて汚れの分解を試してみた。テストは1回にサンマ
4匹を焼き、5回続けたのち、30分間の空焼きで汚れの
分解を行った。空焼き中、調理室内壁の温度は30分後に
280〜400℃まで上昇する。これを1サイクルとして繰り
返すと、空焼き中の低温(280〜300℃程度)部にはター
ル残渣が残るが、全体として従来に比べて良好に浄化が
できることがわかった。ただし、ここに用いた被膜は、
表中、No.4のものである。Next, the saury was actually baked in the cooker shown in FIG. In the test, four saury were baked at a time, and after continuing five times, the soil was decomposed by baking for 30 minutes. During empty baking, the temperature of the cooking indoor wall will be 30 minutes later
Increase to 280-400 ° C. When this was repeated as one cycle, it was found that tar residues remained in the low temperature (about 280 to 300 ° C.) portion during the baking, but it was found that the purification could be better as a whole as compared with the conventional method. However, the coating used here is
No. 4 in the table.
発明の効果 以上のように本発明の塗料硬化被膜およびそれを有す
る調理器によれば、次の効果が得られる。Effects of the Invention As described above, according to the cured paint film of the present invention and the cooking device having the same, the following effects can be obtained.
(1) 本発明の塗料硬化被膜はポリボロチタノシロキ
サンまたはポリボロシロキサンと、繊維状の無機物と、
銅の化合物の一種以上と、溶剤とを混合した塗料を焼成
硬化するので、空気の供給されやすい多孔質被膜とな
り、しかも触媒として対還元性に強い酸化第二銅を含有
しているので触媒活性が高く、かつ触媒活性劣化の少な
いものである。(1) The cured coating film of the present invention comprises a polyborotitanosiloxane or polyborosiloxane, a fibrous inorganic substance,
Baking and hardening paint mixed with one or more copper compounds and a solvent, resulting in a porous film that can be easily supplied with air, and because it contains cupric oxide, which has a strong reducibility as a catalyst, catalytic activity And the catalyst activity is less deteriorated.
(2) 本発明の調理器は金属多孔体表面に前記(1)
記載の塗料硬化被膜を形成した壁面材を調理室内に少な
くとも一面有しているので、調理中に発生する汚れを良
好に浄化できる。(2) The cooker according to the present invention is characterized in that (1)
Since the cooking chamber has at least one surface of the wall material on which the above-described paint cured film is formed, dirt generated during cooking can be satisfactorily purified.
第1図は本発明による塗料硬化被膜を金属多孔体に形成
した壁面材の拡大断面図、第2図は同じく塗料硬化被膜
を形成した壁面材の拡大正面図、第3図(a)は壁面材
を調理室内壁に適用した調理器の斜視図、第3図(b)
は第3図(a)におけるA部の拡大正面図である。 1……ポリボロチタノシロキサンの焼成硬化物、2……
シリカ・アルミナ繊維(繊維状の無機物)、3……酸化
第二銅、4……アルミニウム長繊維(金属多孔体)、5
……壁面材、6……調理器。FIG. 1 is an enlarged cross-sectional view of a wall material in which a cured paint film according to the present invention is formed on a porous metal body, FIG. 2 is an enlarged front view of the same wall material having a cured paint film formed thereon, and FIG. Fig. 3 (b) is a perspective view of a cooker in which ingredients are applied to a cooking chamber inner wall.
FIG. 4 is an enlarged front view of a portion A in FIG. 1 ... baked and cured product of polyborotitanosiloxane, 2 ...
Silica / alumina fiber (fibrous inorganic material), 3 ... cupric oxide, 4 ... aluminum long fiber (porous metal), 5
... wall materials, 6 ... cookers.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 FI F24C 14/00 F24C 14/00 C (72)発明者 脇 真起子 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 平2−53871(JP,A) 特開 平3−174246(JP,A) (58)調査した分野(Int.Cl.6,DB名) A47J 36/02 B01J 21/00 - 38/74 B05D 5/00 C09D 183/14 F24C 14/00──────────────────────────────────────────────────続 き Continued on the front page (51) Int.Cl. 6 Identification code FI F24C 14/00 F24C 14/00 C (72) Inventor Makiko Waki 1006 Ojidoma, Kadoma City, Osaka Matsushita Electric Industrial Co., Ltd. 56) References JP-A-2-53871 (JP, A) JP-A-3-174246 (JP, A) (58) Fields investigated (Int. Cl. 6 , DB name) A47J 36/02 B01J 21/00 -38/74 B05D 5/00 C09D 183/14 F24C 14/00
Claims (2)
構成されるポリボロチタノシロキサンまたはシリコン、
ボロンおよび酸素から構成されるポリボロシロキサン
と、繊維状の無機物と、酸化第二銅、炭酸銅、水酸化銅
および酢酸銅のうちの一種以上の銅の化合物と、前記ポ
リボロチタノシロキサンまたはポリボロシロキサンを溶
解する溶剤とを混合した塗料を焼成硬化してなる塗料硬
化被膜。1. A polyborotitanosiloxane or silicon composed of silicon, boron, titanium and oxygen,
A polyborosiloxane composed of boron and oxygen, a fibrous inorganic substance, cupric oxide, copper carbonate, a compound of one or more copper of copper hydroxide and copper acetate, and the polyborotitanosiloxane or A paint cured film formed by baking and curing a paint mixed with a solvent that dissolves polyborosiloxane.
被膜を形成した壁面材を調理室内に少なくとも一面有す
る調理器。2. A cooker having at least one wall surface material in which a paint cured film according to claim 1 is formed on the surface of a porous metal body.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2097956A JP2833142B2 (en) | 1990-04-13 | 1990-04-13 | Paint cured film and cooker having the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2097956A JP2833142B2 (en) | 1990-04-13 | 1990-04-13 | Paint cured film and cooker having the same |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03296439A JPH03296439A (en) | 1991-12-27 |
JP2833142B2 true JP2833142B2 (en) | 1998-12-09 |
Family
ID=14206121
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2097956A Expired - Fee Related JP2833142B2 (en) | 1990-04-13 | 1990-04-13 | Paint cured film and cooker having the same |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2833142B2 (en) |
-
1990
- 1990-04-13 JP JP2097956A patent/JP2833142B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH03296439A (en) | 1991-12-27 |
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