JPS62186132A - Cooking unit - Google Patents
Cooking unitInfo
- Publication number
- JPS62186132A JPS62186132A JP61027160A JP2716086A JPS62186132A JP S62186132 A JPS62186132 A JP S62186132A JP 61027160 A JP61027160 A JP 61027160A JP 2716086 A JP2716086 A JP 2716086A JP S62186132 A JPS62186132 A JP S62186132A
- Authority
- JP
- Japan
- Prior art keywords
- cooking
- cooking chamber
- base material
- elements
- covering 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.)
- Granted
Links
- 238000010411 cooking Methods 0.000 title claims abstract description 42
- 239000000463 material Substances 0.000 claims abstract description 17
- 229910052751 metal Inorganic materials 0.000 claims abstract description 14
- 230000005855 radiation Effects 0.000 claims abstract description 10
- 239000011347 resin Substances 0.000 claims abstract description 6
- 229920005989 resin Polymers 0.000 claims abstract description 6
- 239000002131 composite material Substances 0.000 claims abstract description 5
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 3
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 3
- 229910052761 rare earth metal Inorganic materials 0.000 claims abstract description 3
- 229910052802 copper Inorganic materials 0.000 claims abstract 2
- 229910052726 zirconium Inorganic materials 0.000 claims abstract 2
- 239000002184 metal Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 abstract description 5
- 230000010718 Oxidation Activity Effects 0.000 abstract description 2
- 150000002430 hydrocarbons Chemical class 0.000 abstract description 2
- 238000004140 cleaning Methods 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 230000003647 oxidation Effects 0.000 abstract 1
- 238000007254 oxidation reaction Methods 0.000 abstract 1
- 238000000576 coating method Methods 0.000 description 17
- 239000011248 coating agent Substances 0.000 description 16
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 8
- 210000003298 dental enamel Anatomy 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 4
- 240000008415 Lactuca sativa Species 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 229910052593 corundum Inorganic materials 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 235000012045 salad Nutrition 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- 229910001845 yogo sapphire Inorganic materials 0.000 description 3
- 230000000694 effects Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004534 enameling Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
Landscapes
- Catalysts (AREA)
Abstract
Description
【発明の詳細な説明】
産業上の利用分野
本発明は、オープン、グリルなどの家庭用あるいは業務
用の電気を熱源とした調理器に関する。DETAILED DESCRIPTION OF THE INVENTION Field of the Invention The present invention relates to cooking appliances such as open cookers, grills, and the like that use electricity as a heat source for domestic or commercial use.
従来の技術
従来オーブンやグリルにおける加熱手段は、調理室内に
シーズヒータを組込んだものや、同じく調理室内でガス
バーナで輻射体を赤熱させるものなど、熱源に応じて種
々の手段が使用されていた。Conventional technology Conventional heating means for ovens and grills have been various depending on the heat source, such as a sheathed heater built into the cooking chamber or a radiant heated by a gas burner inside the cooking chamber. .
電気の場合に限定すれば、前記の如くシーズヒータを組
込んだものが圧倒的に多く、一部平面ヒータを用いたも
のがある。In the case of electricity, most of them incorporate sheathed heaters as mentioned above, and some use planar heaters.
一方調理中に発生する油の分解については、自己浄化能
(以下S、C0と称す)をもつS、C,被膜を調理室内
面に設は調理中に発生する油を分解する手段をとってい
る。On the other hand, in order to decompose the oil generated during cooking, we installed an S, C, film with self-purifying ability (hereinafter referred to as S, C0) inside the cooking chamber as a means to decompose the oil generated during cooking. There is.
発明が解決しようとする問題点
前記の従来技術における問題点は、加熱手段についてシ
ーズヒータの場合、
(1) ヒータ自身の加熱有効面積が、調理室内天井
面積に対し極めて小さく、調理速度も遅く、熱源の有効
利用ができない。Problems to be Solved by the Invention The problems with the prior art described above are that, in the case of a sheathed heater as a heating means, (1) the effective heating area of the heater itself is extremely small relative to the ceiling area of the cooking chamber, and the cooking speed is slow; Heat source cannot be used effectively.
平面ヒータの場合、
(2)加熱有効面積は、調理室内天井面積にほぼ等しく
問題はないが、調理室内天井面に施されているS、C,
被覆面の耐熱性がそれほど高くないということから、ヒ
ータや調理室内面の温度を高くすることができなくなる
。よって加熱有効面積を、充分に生かせない。又、調理
室内面の赤外線輻射率が、それほど高くないという事も
上記構成においては問題となる。In the case of a flat heater, (2) the effective heating area is almost equal to the ceiling area of the cooking chamber, so there is no problem;
Since the heat resistance of the coated surface is not very high, it becomes impossible to raise the temperature of the heater or the inside of the cooking chamber. Therefore, the effective heating area cannot be fully utilized. Another problem with the above configuration is that the infrared emissivity of the inner surface of the cooking chamber is not so high.
一方、S、C0の観点からは、
C3) S、C,能がホウロウ処理により調理室内の
天井面に施されていることから、耐熱温度が約400°
Cで、天井面の温度がそれ以上になるとホウロウのガラ
ス成分が溶けるとか、基材から剥離するなどの現象が発
生する懸念がある。ホウロウは膜厚も数100μmと厚
く、その点からも熱サイクルにより剥離しやすいことも
あり、当然の事であるが剥離すればS、C,能が低下す
る。On the other hand, from the perspective of S, C0, C3) Since S, C, Noh is applied to the ceiling surface of the cooking chamber by enameling, the heat resistance temperature is approximately 400°.
In C, if the temperature of the ceiling surface exceeds this temperature, there is a concern that phenomena such as the glass component of the enamel melting or peeling from the base material may occur. The film thickness of enamel is as thick as several 100 μm, and from this point of view, it is easy to peel off due to thermal cycles, and as a matter of course, if it peels off, the S, C, and performance will decrease.
問題点を解決するための手段
と記問題を解決するために、本発明は、平面ヒータを用
いたオーブンあるいはグリルなどの調理器において、前
記調理器の調理室を形成する金属基材と、この金属基材
から成る調理室の内面に、油分解能と赤外線輻射能とを
合わせもつ被膜を形成する構成とし、前記被膜を、希土
類元素と金属元素の複合酸化物であるペロブスカイト型
酸化物と、Zr 、Ti 、 Si 、八4 の元素群
から選択される少くとも一皿以上の酸化物と、Fe 、
Co 、 Ni 、 Mn。Means for Solving the Problems In order to solve the problems, the present invention provides a cooking device such as an oven or a grill using a plane heater, which includes a metal base material forming a cooking chamber of the cooking device; A coating having both oil-decomposing ability and infrared radiation ability is formed on the inner surface of the cooking chamber made of a metal base material, and the coating is made of perovskite-type oxide, which is a composite oxide of a rare earth element and a metal element, and Zr. , Ti, Si, at least one oxide selected from the element group 84, and Fe,
Co, Ni, Mn.
Cu の元素群から選択される少なくとも一種以上の酸
化物と、ボロシロキサン樹脂の硬化体とで構成するもの
とした。It is composed of at least one oxide selected from the Cu element group and a cured body of borosiloxane resin.
作 用 上記手段により、本発明は以下の様な作用を有する。For production By means of the above means, the present invention has the following effects.
(1)ペロブスカイト型複合酸化物をはじめとして、前
記被膜を構成している酸化物ならびにボロシロキサン樹
脂の硬化体は、耐熱温度が少くともt oo。(1) The perovskite-type composite oxide and other oxides constituting the film and the cured product of the borosiloxane resin have a heat resistance temperature of at least 200 yen.
°C近くから、それ以上であり、しかも金属基材との密
着性も優れており、剥離の懸念もない上にヒータ温度や
調理室内面温度を従来に比べてはるかに高くできる。℃ or higher, has excellent adhesion to the metal base material, there is no fear of peeling, and the heater temperature and cooking chamber inner temperature can be much higher than conventional methods.
(2)ペロブスカイト型複合酸化物は、白金に匹敵する
酸化活性を有し、調理中に発生する油分である炭化水素
化合物等を酸化分解するために、被膜にS、C1能を付
与することができる。しかも調理室内面温度を従来より
高くできるために油の分解速度はより促進される。(2) Perovskite-type composite oxides have an oxidation activity comparable to that of platinum, and can impart S and C1 abilities to the film in order to oxidize and decompose oily hydrocarbon compounds generated during cooking. can. Moreover, since the internal temperature of the cooking chamber can be made higher than before, the rate of oil decomposition is further accelerated.
(3)被膜は、赤外線の輻射率が高く、波長2〜7μm
で輻射率が約0.8、波長7〜30μmで輻射率が約0
.9以上となっている。金属基材で輻射率が0.1〜0
.3程度であるから、オーブンやグリルの様な輻射型の
調理器においては、輻射率が高い事は、非常に有利であ
る。(3) The coating has a high emissivity of infrared rays, with a wavelength of 2 to 7 μm.
The emissivity is approximately 0.8, and the emissivity is approximately 0 at a wavelength of 7 to 30 μm.
.. It is 9 or more. Metal base material with emissivity of 0.1 to 0
.. Since the radiation rate is about 3, it is very advantageous to have a high radiation rate in radiation type cooking devices such as ovens and grills.
4)上記被膜の膜厚は平均10pmと非常に薄いために
、熱サイクルによる膜自身のわれなどはない。4) Since the film thickness of the above film is very thin at an average of 10 pm, there is no cracking of the film itself due to thermal cycles.
実施例 以下、本発明の実施例について説明する。Example Examples of the present invention will be described below.
前記被膜は塗装方式で金属基村上に形成される為に、そ
の時の作業は簡単には、
(1)膜構成材料の塗料化、(2)金属基材の脱脂、(
3)塗装、(4焼付という工程をとる。よって以下に、
材料の選択及び塗料化、塗装方法、焼付条件について述
べ、更に被膜の物性、S、C,能、等について説明する
。Since the film is formed on the metal substrate by a painting method, the work at that time is simply: (1) turning the film constituent material into a paint, (2) degreasing the metal substrate, (
3) Painting, (4) Baking process.Therefore, below:
The selection of materials, coating, coating methods, and baking conditions will be described, and the physical properties of the film, S, C, performance, etc. will be explained.
材料の選定 その他酸化物として ZrO2 1j203 Fe203 llMn○2・Cu。Material selection Other oxides: ZrO2 1j203 Fe203llMn○2・Cu.
ボロシロキサン樹脂として を選定した。第1表に詳細を示した。As borosiloxane resin was selected. Details are shown in Table 1.
第1表 塗料化 第2表に塗料化の為の各材料の配合比を示した。Table 1 Paint Table 2 shows the blending ratio of each material for making the paint.
第2表
上記組成のものを撹拌機(アトライタ)で約2時間撹拌
し塗料化した。Table 2 The above-mentioned composition was stirred for about 2 hours using an agitator (attritor) to form a paint.
塗装・焼付
金属基材は予め溶剤脱脂又は、アルカリ脱脂を行い、ス
プレ一方式で塗装を行う。焼付けは200〜250°C
で30分さらに400’Cで30分とした。Painted/baked metal substrates are degreased with solvent or alkaline in advance, and then painted using a one-way spray method. Baking at 200-250°C
The temperature was further increased to 400'C for 30 minutes.
上記の工程により、調理室内の天井面及び底面に被膜を
形成した。(第1図)
被膜の物性
第3表に本実施例による被膜の物性を示し、又第2図に
は約500°Cでの赤外線の分光輻射率を示した。Through the above steps, a coating was formed on the ceiling and bottom surfaces of the cooking chamber. (FIG. 1) Physical Properties of Coating Table 3 shows the physical properties of the coating according to this example, and FIG. 2 shows the infrared spectral emissivity at about 500°C.
第3表 * 焼成条件で変化。Table 3 *Varies depending on firing conditions.
上記特性はホウロウでは得られないものである。The above characteristics cannot be obtained with enamel.
第2図かられかるように、被膜の輻射率が0.8〜0.
9と高いが、これはF e 203 ・M n O2・
Cu O。As can be seen from Figure 2, the emissivity of the coating is 0.8 to 0.
Although it is high at 9, this is F e 203 ・M n O2 ・
Cu O.
Al2O3、ZrO2の様な酸化物による赤外線の拡散
・吸収をうまく利用したもので、特にFe2O3・Mn
O2・Cu Oは2〜7μmの短波長側の輻射率を著し
く向上させ、Al2O3、ZrO2はどちらかといえば
7〜30μmの長波長側の輻射率を向上させているもの
である。It makes good use of the diffusion and absorption of infrared rays by oxides such as Al2O3 and ZrO2, especially Fe2O3 and Mn.
O2.CuO significantly improves the emissivity on the short wavelength side of 2 to 7 μm, and Al2O3 and ZrO2 rather improve the emissivity on the long wavelength side of 7 to 30 μm.
S、C,特性
第3図に名種表面のS、C,特性を示した。テストの手
段は、ホットプレートを任意温度に設定し、それにより
、各種表面のサンプルの温度を、一定にした。そこへ、
サラダ油を一定量滴下し一定時間放置後、またサラダ油
を滴下した。この操作を10回繰り返し、テスト前後の
サンプ、ルの重量増分を計り、これをサラダ油の残査分
とした。よって、この残査分が少い程、S、C,能が優
れていると言える。S, C, characteristics Figure 3 shows the S, C, characteristics of the surface of the famous species. The test was carried out by setting a hot plate at an arbitrary temperature, thereby keeping the temperature of the samples on various surfaces constant. There,
After dropping a certain amount of salad oil and leaving it for a certain period of time, another drop of salad oil was added. This operation was repeated 10 times, and the weight increase of the sample before and after the test was measured, and this was taken as the residual amount of salad oil. Therefore, it can be said that the smaller this residual amount is, the better the S, C, and performance are.
第3図から、本実施例による被膜のS、C0特性は従来
のS、C,ホウロウよりも優れていることがわかる。It can be seen from FIG. 3 that the S, C0 characteristics of the coating according to this example are superior to those of conventional S, C, and enamel.
調理器の調理室内の温度上昇速度
オーブンやグリルなど調理器の調理室内の温度上昇の速
度は速ければ速い程よい。調理時間の短縮化、省エネに
なるからである。第4図に、オーブン室内の温度上昇曲
線の一例を示した。これからもわかる様に従来使われて
いるS、C,ホウロウを施したオーブンに比べ、本実施
例による被膜を施したオーブンの方が、はるかに温度上
昇が速い。Speed of temperature rise in the cooking chamber of a cooking device The faster the temperature rise in the cooking chamber of a cooking device such as an oven or grill, the better. This is because it shortens cooking time and saves energy. FIG. 4 shows an example of a temperature rise curve inside the oven chamber. As can be seen from this, the temperature rises much faster in the oven coated with the film of this example than in the conventionally used ovens coated with S, C, and enamel.
この理由は、被膜の輻射率が高いこと、耐熱性が優れて
いるために、ヒータ自身の温度を上げることができるこ
とにある。The reason for this is that the coating has a high emissivity and excellent heat resistance, so the temperature of the heater itself can be raised.
発明の詳細 な説明した様に本発明によれば以下の効果が得られる。Details of the invention As explained above, according to the present invention, the following effects can be obtained.
(1)材料の塗料化、塗装、焼成という比較的簡単な工
程で安価に、前記被膜が形成できて、コストパフォーマ
ンスが高い。(1) The film can be formed at low cost through a relatively simple process of converting the material into paint, painting, and baking, and has high cost performance.
(2) S、(、能が高いために、調理器から発生す
るガスをクリーン化できて衛生的である。(2) Due to its high performance, the gas generated from the cooker can be cleaned and it is hygienic.
(3)赤外線輻射率が高く、かつ憂れた塗膜物性を有す
るので、調理器室内の温度上昇が速くなり調理時間の短
縮化、省エネ、さらには、調理メニューの拡大化が図れ
る。(3) Since the infrared emissivity is high and the coating film has poor physical properties, the temperature in the cooking chamber increases quickly, shortening cooking time, saving energy, and further expanding the cooking menu.
第1図は本発明の一実施例における調理器の被膜と金属
基材の密着部の要部拡大断面図、第2図は同調理器の被
膜の500℃における赤外線分光輻射特性図、第3図は
各種表面の各温度でのS、C9特性図、第4図は同調理
器と従来の調理器の調理室内の温度上昇図である。
1・・・・ボロシロキサン樹脂硬化体、2・・・・・・
La0,9CeQ、lCoO3,3−−−・Al2O3
またはZrO2またはFe2O3”MnO,)・CuO
1jl−・・金属基材、5・・・・・・被膜、6・・・
・・・金属基材、7・・・・・・被膜、9・・・・・・
被膜。
代理人の氏名 弁理士 中 尾 敏 男 ほか1名ノー
ーーボロVロキプン市ti*cイ乙伴・第2図
淳J良(〃割りFIG. 1 is an enlarged cross-sectional view of the main part of the contact area between the coating of the cooking device and the metal base material in one embodiment of the present invention, FIG. 2 is an infrared spectral radiation characteristic diagram of the coating of the cooking device at 500°C, The figures are S and C9 characteristic diagrams at various temperatures of various surfaces, and FIG. 4 is a temperature rise diagram in the cooking chambers of the same cooker and a conventional cooker. 1...Borosiloxane resin cured body, 2...
La0,9CeQ, lCoO3,3---・Al2O3
or ZrO2 or Fe2O3”MnO, )・CuO
1jl-...Metal base material, 5...Coating, 6...
...Metal base material, 7...Coating, 9...
Coating. Name of agent: Patent attorney Toshio Nakao and one other person
Claims (1)
し、前記被膜は希土類元素と金属元素の複合酸化物であ
るペロブスカイト型酸化物と、Zr、Ti、Si、Al
の元素群から選択される少なくとも一種の酸化物と、F
e、Co、Ni、Mn、Cuの元素群から選択される少
なくとも一種以上の酸化物と、ボロシロキサン樹脂の硬
化体とで構成される、油分解能と赤外線輻射能とを合わ
せもつ調理器。A film is formed on the surface of a metal base material forming a cooking chamber of a cooking device, and the film is made of a perovskite type oxide, which is a composite oxide of a rare earth element and a metal element, and Zr, Ti, Si, and Al.
at least one oxide selected from the element group F
A cooking device having both oil-decomposing ability and infrared radiation ability, which is composed of at least one oxide selected from the group of elements e.g., Co, Ni, Mn, and Cu and a cured product of borosiloxane resin.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61027160A JPH0658174B2 (en) | 1986-02-10 | 1986-02-10 | Cooking device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61027160A JPH0658174B2 (en) | 1986-02-10 | 1986-02-10 | Cooking device |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS62186132A true JPS62186132A (en) | 1987-08-14 |
JPH0658174B2 JPH0658174B2 (en) | 1994-08-03 |
Family
ID=12213301
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP61027160A Expired - Fee Related JPH0658174B2 (en) | 1986-02-10 | 1986-02-10 | Cooking device |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0658174B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08117596A (en) * | 1994-10-27 | 1996-05-14 | Matsushita Seiko Co Ltd | Method for carrying titanium dioxide particle |
-
1986
- 1986-02-10 JP JP61027160A patent/JPH0658174B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08117596A (en) * | 1994-10-27 | 1996-05-14 | Matsushita Seiko Co Ltd | Method for carrying titanium dioxide particle |
Also Published As
Publication number | Publication date |
---|---|
JPH0658174B2 (en) | 1994-08-03 |
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