JPH03296439A - Paint cured film and cooker having the same - Google Patents
Paint cured film and cooker having the sameInfo
- Publication number
- JPH03296439A JPH03296439A JP2097956A JP9795690A JPH03296439A JP H03296439 A JPH03296439 A JP H03296439A JP 2097956 A JP2097956 A JP 2097956A JP 9795690 A JP9795690 A JP 9795690A JP H03296439 A JPH03296439 A JP H03296439A
- Authority
- JP
- Japan
- Prior art keywords
- film
- paint
- copper
- oxygen
- polyborotitanosiloxane
- 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.)
- Granted
Links
- 239000003973 paint Substances 0.000 title claims abstract description 23
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 claims abstract description 32
- 238000010411 cooking Methods 0.000 claims abstract description 25
- 239000000463 material Substances 0.000 claims abstract description 15
- 229910052751 metal Inorganic materials 0.000 claims abstract description 12
- 239000002184 metal Substances 0.000 claims abstract description 12
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229960004643 cupric oxide Drugs 0.000 claims abstract description 11
- 239000001301 oxygen Substances 0.000 claims abstract description 11
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 11
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000005749 Copper compound Substances 0.000 claims abstract description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910052796 boron Inorganic materials 0.000 claims abstract description 6
- 150000001880 copper compounds Chemical class 0.000 claims abstract description 6
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 6
- 239000010703 silicon Substances 0.000 claims abstract description 6
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 229940116318 copper carbonate Drugs 0.000 claims abstract description 4
- GEZOTWYUIKXWOA-UHFFFAOYSA-L copper;carbonate Chemical compound [Cu+2].[O-]C([O-])=O GEZOTWYUIKXWOA-UHFFFAOYSA-L 0.000 claims abstract description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000010936 titanium Substances 0.000 claims abstract description 3
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 3
- 239000010949 copper Substances 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 3
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 2
- 229910052802 copper Inorganic materials 0.000 claims description 2
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims 1
- 230000003197 catalytic effect Effects 0.000 abstract description 15
- 239000000835 fiber Substances 0.000 abstract description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 10
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 5
- 239000000377 silicon dioxide Substances 0.000 abstract description 5
- 239000011230 binding agent Substances 0.000 abstract description 4
- 239000000356 contaminant Substances 0.000 abstract 3
- 229940126214 compound 3 Drugs 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 239000003921 oil Substances 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 8
- 238000000354 decomposition reaction Methods 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 240000008415 Lactuca sativa Species 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 235000012045 salad Nutrition 0.000 description 3
- 241001149724 Cololabis adocetus Species 0.000 description 2
- JJLJMEJHUUYSSY-UHFFFAOYSA-L Copper hydroxide Chemical compound [OH-].[OH-].[Cu+2] JJLJMEJHUUYSSY-UHFFFAOYSA-L 0.000 description 2
- 239000005750 Copper hydroxide Substances 0.000 description 2
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 229910001956 copper hydroxide Inorganic materials 0.000 description 2
- RCJVRSBWZCNNQT-UHFFFAOYSA-N dichloridooxygen Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 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
- 229910000314 transition metal oxide Inorganic materials 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 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
- 239000002313 adhesive film Substances 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 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
- BERDEBHAJNAUOM-UHFFFAOYSA-N copper(I) oxide Inorganic materials [Cu]O[Cu] BERDEBHAJNAUOM-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
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 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
- 239000000945 filler Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000010438 heat treatment Methods 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
- 235000012054 meals Nutrition 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000006864 oxidative decomposition reaction Methods 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
- 238000010998 test method Methods 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 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)
Abstract
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。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to a cured paint coating for cleaning dirt generated from cooking appliances for household use, business use, etc., 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“C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、訓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。Conventional technology In the past, there were mainly three methods for cleaning dirt generated from cooking appliances.
The second method is to heat the cooking chamber to ~500"C to thermally decompose the dirt. The second method is to form a film containing a catalyst such as transition metal oxide or zeolite that has a catalytic action on the wall surface of the cooking chamber and decompose the dirt through the catalytic action. The third method is to form a non-adhesive film on the inner wall of the training room and wipe off any dirt that has adhered to it.
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 techniques have 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
。With the first thermal decomposition method, there are issues with thermal deterioration and safety of electronic components due to the high temperature being maintained for a long period of time, while with the second decomposition method using catalytic action, the catalyst is covered with the binder in the film. There are problems in that high activity cannot be obtained and the decomposition of dirt is incomplete, and a part of the catalyst is reduced and deteriorated during the reaction. The problem is that the heat resistance temperature of the metal is low.
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。The present invention aims to solve these problems and provide a cured paint film that cleans dirt due to catalytic action, and a cooking appliance 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
(Cub)、炭酸銅(CuCOl)、水酸化銅[Cu
(OH)z ]および酢酸銅[Cu (OOCCH3)
z ]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 objects, 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 inorganic substances, cupric oxide (Cub), copper carbonate (CuCOl), copper hydroxide [Cu
(OH)z ] and copper acetate [Cu (OOCCH3)
A coating mixture of one or more of the copper compounds selected from the following and a solvent is fired and cured to form a porous cured coating film having catalytic action. Further, this cured paint film is formed on the surface of the metal porous body to form a wall material, and the cooking appliance has at least one wall material inside 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。Effect By the above means, polyborotitanosiloxane or polyborosiloxane is a binder, and although it is difficult to form a film by itself even if it is baked and cured, it is easy to form a film by adding an appropriate amount of filler. Moreover, fibrous inorganic materials tend to form porous films, and in particular, fibrous inorganic materials increase porosity. The reason is,
This is because since the fibers are straight, they tend to intertwine with each other in the coating, creating voids.
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 that decomposes oil stains, which are typical stains caused by cooking, through catalytic action, and the presence of oxygen is important. The oxygen is supplied from the air, and in order to take in as much oxygen as possible, a porous film is desired. 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3
00〜350℃)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
の遷移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’C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。Furthermore, cupric oxide, which acts as a catalyst, is prepared by impregnating the powder with oil (e.g. salad oil) and heating it in the air (approximately 3
(00 to 350℃), the oil is oxidized and decomposed, but the structure does not change before and after the reaction.Other transition metal oxides such as manganese and cobalt are easily reduced during the reaction and their structure changes and their activity decreases. Even when there is no structural change, the activity is lower than that of cupric oxide, and it is invulnerable as a catalyst unless it is combined with other elements to improve its resistance to reduction. On the other hand, cupric oxide also has catalytic activity, and even if it is reduced to cuprous oxide during the reaction, it easily converts to cupric oxide if the temperature is above 300'C in air. As mentioned above, since the film is porous, cupric oxide can easily take in oxygen and catalytically oxidize and decompose oil, and can also prevent deterioration. It is.
また炭酸銅、水酸化銅、酢M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
COよ、H,O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。In addition, copper carbonate, copper hydroxide, and copper vinegar decompose during firing and hardening to become cupric oxide. It is easy to create voids 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, the metal porous body with the above film formed on its surface has a pore diameter of several hundreds of micrometers and has continuous pores, so it is more effective at absorbing and diffusing oil than conventional porous bodies with discontinuous pores due to foaming. It has much better properties and oxygen diffusivity. Therefore, it is suitable for exhibiting the catalytic action of the above-mentioned film.
以上のような触媒作用を存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 a porous metal body to serve as a wall material and placing it inside a cooking appliance, it becomes possible to catalytically decompose and purify dirt caused by 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
。EXAMPLE An example of the present invention will be described below 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m(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 paint film according to the present invention and a wall material in which the cured paint film is formed on the surface of a porous metal body.
is silica/alumina fiber, 3 is oxidized di(CuO),
4 is 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lOOμm、アルミニウム長繊維4は直径が数10〜
数100μm、長さが数10閣、被膜の厚さは約20μ
m以下である。Figure 2 is an enlarged view of the aluminum long fiber wall material 5 shown in Figure 1 with a cured paint film formed on its surface. ~
The aluminum long fiber 4 has a diameter of several 10 μm.
Several 100 μm in length, several tens of micrometers in length, and the thickness of the coating is approximately 20 μm.
m 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図ら)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バ
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 cooking device (6) in which the wall material (5) shown in FIG. 2 is installed in the cooking chamber, and FIG.
It is an enlarged front view of the A section in figure (a), that is, the wall material (5). In Figures 3 and 3), (7) is an aluminum expanded metal provided to reinforce the aluminum long fibers, and a cured paint film is also formed on its surface.
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 cured paint film shown in FIGS. 1, 2, and 3 and the cooking appliance having the same will be explained.
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0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100膳×1
00閣×0.7閣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、350℃の電気炉内で15分間放置を1サイク
ルとした0表中FkL1〜7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°Cl2O分で行った0表中、隘5〜
7の銅化合物は焼成硬化によりCuOとなる。First, the paint effect film will be explained. As a conventional example, a film having a catalytic action consisting of an inorganic phosphate and a metal oxide was used. The table below shows the catalyst in the film and the results of the decomposition and purification test using salad oil as a representative example of oil.The 0 decomposition and purification test involves forming a hardened paint film on the surface of a porous body made of aluminum long fiber laminate. 100 meals x 1
Using a test piece of 00 × 0.7 Kaku, the test method was to drop about 0.1 g of salad oil on the test piece at 5 points, and leave it in an electric furnace at 350°C for 15 minutes for one cycle. In Table 0, FkL1 to 7 are according to the present invention, and 90 parts by weight of polyborotitanosiloxane and 20 parts by weight of silica/alumina fiber are common, so they are not included in the table.
In addition, the firing was performed at 450°Cl2O minutes.
The copper compound No. 7 becomes CuO by firing and hardening.
以下余白
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0表中、隘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、N
a4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サベクルでタール残渣があったこ
とも裏付けとなる。Below Margin As is clear from the above table, it is preferable to have a large amount of CuO, but if it is too large, the film becomes brittle, so 60-100 parts by weight is preferable.
It can be seen that the catalytic action of CuO and the overall structure of the porous test piece contribute to decomposition and purification. In the table, N
This is also supported by the fact that when the A4 coating was formed on an aluminum flat plate and a decomposition and purification test was conducted, tar residue was 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、例えば同しく
活性の高いMro、はMr20.へと還元され活性が低
下した。Next, it was confirmed by X-ray diffraction that the catalyst CuO does not change its structure before and after the reaction.For example, Mr20. 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。Regarding the fibrous inorganic substance in the coating, in addition to silica and alumina, zirconia, silicon carbide, and carbon can also be used, and long fibers of these can be crushed into short pieces.
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。Further, as for the metal porous body, stainless steel may be used instead of aluminum, and both of these are continuous porous bodies. In the case of stainless steel, the fiber diameter may be smaller than that of aluminum, but both 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。Next, we tried to break down the dirt by actually roasting saury in the cooker shown in Figure 3(a). The test is 4 saury at one time.
After grilling the fish five times in a row, the dirt was broken down by dry baking for 30 minutes. During dry baking, the temperature of the inner wall of the cooking chamber rises to 280 to 400°C after 30 minutes.
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°C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、階4のもの
である。If you repeat this as one cycle, the low temperature (
(about 280 to 300°C), tar residue remains,
Overall, it was found that purification was better than conventional methods. However, the coating used here is that of grade 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, the cured paint film of the present invention and the cooking appliance having the same provide the following effects.
(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存して
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 paint film of the present invention is a mixture of polyborotitanosiloxane or polyborosiloxane, a fibrous inorganic material, one or more copper compounds, and a solvent, and is cured by baking. It becomes a porous film that is easily
Furthermore, since it contains cupric oxide, which has strong resistance to reduction, as a catalyst, it has high catalytic activity and little deterioration of catalytic activity.
(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) Since the cooking device of the present invention has at least one wall material in the cooking chamber on which the cured paint film described in (1) above is formed on the surface of the metal porous body, dirt generated during cooking can be effectively cleaned. can.
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図は同しく塗料硬化被膜
を形成した壁面材の拡大正面図、第311ffl(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
1D(b)は第3図(a)におけるA部の拡大正面図で
ある。
■・・・・・・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&li維(金属多孔体)、5・・・・・・壁
面材、6・・・・・・調理器。Fig. 1 is an enlarged sectional view of a wall material in which a cured paint film according to the present invention is formed on a metal porous body, Fig. 2 is an enlarged front view of a wall material in which a cured paint film is also formed, and Fig. 311ffl(a)
Figure 3 is a perspective view of a cooking appliance in which wall material is applied to the walls of the cooking chamber.
1D(b) is an enlarged front view of section A in FIG. 3(a). ■...Calcination cured product of polyborotitanosiloxane, 2...Silica/alumina fiber (fibrous inorganic substance), 3...Cupric oxide, 4... ... Aluminum length & Li fiber (metal porous body), 5 ... Wall material, 6 ... Cooking device.
Claims (2)
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) Polyborotitanosiloxane composed of silicon, boron, titanium and oxygen or polyborosiloxane composed of silicon, boron and oxygen, fibrous inorganic substance, cupric oxide, copper carbonate, hydroxide A cured paint film obtained by baking and curing a paint mixture of one or more copper compounds among copper and copper acetate, and the polyborotitanosiloxane or a solvent that dissolves the polyborosiloxane.
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 cooking device having at least one wall material in the cooking chamber, the wall material having the cured paint film according to claim 1 formed on the surface of a metal porous 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 true JPH03296439A (en) | 1991-12-27 |
JP2833142B2 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 |
---|---|
JP2833142B2 (en) | 1998-12-09 |
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