JPH0343474A - Heat-resistant coating film and heating cooker coated with the same film - Google Patents
Heat-resistant coating film and heating cooker coated with the same filmInfo
- Publication number
- JPH0343474A JPH0343474A JP17954189A JP17954189A JPH0343474A JP H0343474 A JPH0343474 A JP H0343474A JP 17954189 A JP17954189 A JP 17954189A JP 17954189 A JP17954189 A JP 17954189A JP H0343474 A JPH0343474 A JP H0343474A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- resistant coating
- coating
- film
- coating 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.)
- Pending
Links
- 238000000576 coating method Methods 0.000 title claims abstract description 39
- 239000011248 coating agent Substances 0.000 title claims abstract description 33
- 238000010438 heat treatment Methods 0.000 title claims abstract description 7
- 238000010411 cooking Methods 0.000 claims abstract description 16
- 239000011230 binding agent Substances 0.000 claims abstract description 13
- 150000001875 compounds Chemical class 0.000 claims abstract description 7
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 5
- 239000011521 glass Substances 0.000 claims abstract 3
- 239000000843 powder Substances 0.000 claims abstract 3
- 210000003298 dental enamel Anatomy 0.000 claims description 8
- 239000002131 composite material Substances 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 5
- 239000002775 capsule Substances 0.000 claims 1
- 239000003779 heat-resistant material Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000000037 vitreous enamel Substances 0.000 abstract 1
- 238000000746 purification Methods 0.000 description 13
- 239000010408 film Substances 0.000 description 11
- 239000012528 membrane Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000002845 discoloration Methods 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- 229910000314 transition metal oxide Inorganic materials 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 230000009471 action Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000006356 dehydrogenation reaction Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 241000251468 Actinopterygii Species 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 229910003296 Ni-Mo Inorganic materials 0.000 description 1
- 229910003294 NiMo Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000014633 carbohydrates Nutrition 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000007327 hydrogenolysis reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 229910052914 metal silicate Inorganic materials 0.000 description 1
- VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052961 molybdenite Inorganic materials 0.000 description 1
- CWQXQMHSOZUFJS-UHFFFAOYSA-N molybdenum disulfide Chemical compound S=[Mo]=S CWQXQMHSOZUFJS-UHFFFAOYSA-N 0.000 description 1
- 229910052982 molybdenum disulfide Inorganic materials 0.000 description 1
- DDTIGTPWGISMKL-UHFFFAOYSA-N molybdenum nickel Chemical compound [Ni].[Mo] DDTIGTPWGISMKL-UHFFFAOYSA-N 0.000 description 1
- -1 oil Chemical class 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 229910001404 rare earth metal oxide Inorganic materials 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Cookers (AREA)
- Compositions Of Macromolecular Compounds (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、グリルといった加熱調理器の庫内に
塗布し、調理中に発生した汚れを加熱下で分解・除去す
る機能を持つ耐熱性被膜と前記耐熱性被膜を施した加熱
調理器に関するものである。DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is a heat-resistant coating that is applied to the inside of a heating cooker such as an open cooker or a grill, and has the function of decomposing and removing dirt generated during cooking under heating. The present invention relates to a cooking device provided with the heat-resistant coating.
従来の技術
肉や魚等の調理を行った際に調理器庫内壁に付着する汚
れを加熱下で分解除去する被膜とその被膜を施した調理
器には大別して次の2つの構造があげられる。Conventional technology There are two main types of coatings: coatings that decompose and remove dirt that adheres to the inner walls of cooking appliances under heat when cooking meat, fish, etc., and cooking utensils coated with the coatings, as follows: .
第1は被膜がホーローから威り、ホーロー表面温度で約
450°C以上になるように庫内温度を上げ熱によって
ホーロー表面の汚れを分解するものである。The first method is to raise the internal temperature of the enamel so that the coating heats up from the enamel and the surface temperature of the enamel reaches approximately 450° C. or higher, thereby decomposing dirt on the enamel surface using heat.
第2は、被膜が無機金属のリン酸塩やケイ酸塩やホーロ
ーをバインダーとし、これにMn、Cu。Second, the coating uses inorganic metal phosphate, silicate, or enamel as a binder, and Mn and Cu.
Fe、Co、Ni等の遷移金属酸化物やアルカリ土類酸
化物等を分散させた多孔vII#の場合である。This is the case of porous vII# in which transition metal oxides such as Fe, Co, and Ni and alkaline earth oxides are dispersed.
このような被膜は金属酸化物の触媒作用で油汚れを低温
で燃焼させ分解除去するというものであった。This kind of coating used the catalytic action of metal oxides to burn and decompose oil stains at low temperatures.
発明が解決しようとする課題
しかしながら上記従来の技術には次のような諜題がある
。ホーローでは温度がsoo’c以上になるとクラック
が発生し剥離する。このため鉄基材が腐食し調理器とし
ての使用に耐えなくなる。Problems to be Solved by the Invention However, the above conventional techniques have the following problems. In enamel, cracks occur and peeling occurs when the temperature reaches soo'c or higher. As a result, the iron base material corrodes and becomes unusable as a cooker.
またリン酸塩やケイ酸塩をバインダーとした多孔質膜に
ついては油汚れを完全燃焼させるために油と触媒との接
触面積をふやし被膜中の酸素拡散をよくするため被膜を
できるだけ多孔質にしなければならない。In addition, for porous membranes using phosphates or silicate as a binder, the coating must be made as porous as possible to increase the contact area between the oil and the catalyst and to improve oxygen diffusion within the coating to ensure complete combustion of oil stains. Must be.
しかし多孔質にすると硬度が低くなり剥離したり傷つい
たりし実用上課題がある。また焼は残ったタール成分や
灰分が多孔質の隙間に入り込んで沈着してしまい浄化性
能が徐々に低下する可能性がある。However, if the material is made porous, its hardness decreases and it may peel or be damaged, which poses a practical problem. Furthermore, burning causes residual tar components and ash to enter the porous spaces and settle there, which may gradually reduce purification performance.
上記のように従来技術ではいくつかの課題があるが、本
発明では緻密で硬度の高い被膜上で油汚れを浄化する構
造を取り上げる。As mentioned above, there are some problems with the conventional technology, but the present invention deals with a structure that cleans oil stains on a dense and hard coating.
課題を解決するための手段
上記11題を解決するために、本発明はポリボロシロキ
サン、ポリチタノシロキサンの1種もしくは2種の混合
物をバインダーとし、層状構造を持つ化合物とNi、M
oの複合酸化物とから緻密で平滑で、更に油汚れの酸化
分解力を持つ耐熱性被膜と、前記耐熱性被膜を調理器庫
内壁に塗布し、調理中に調理物から飛散して庫内壁に付
着した汚れを浄化する加熱調理器を提供するものである
。Means for Solving the Problems In order to solve the above 11 problems, the present invention uses one type or a mixture of two of polyborosiloxane and polytitanosiloxane as a binder, and a compound having a layered structure and Ni, M
A heat-resistant coating made of a composite oxide of o, which is dense and smooth, and has the ability to oxidize and decompose oil stains, and the heat-resistant coating is applied to the inner wall of the cooking appliance, and the heat-resistant coating is applied to the inner wall of the cooking appliance to prevent the particles from scattering from the food during cooking. To provide a heating cooker that cleans dirt adhering to food.
作用 本発明による被膜の油汚れ浄化作用について説明する。action The oil stain purifying effect of the film according to the present invention will be explained.
汚れには、油のような高級脂肪酸のトリグリセライド、
タンパク質、炭水化物や塩分、灰分等があげられるが、
ここでは油を代表例として作用を説明する。For stains, triglycerides of higher fatty acids such as oil,
Examples include protein, carbohydrates, salt, ash, etc.
Here, the action will be explained using oil as a representative example.
油の構造を(1)式とすると、浄化に必要な反応は炭素
間結合の切断、二酸化炭素、水への酸化である。If the structure of oil is given by formula (1), the reactions necessary for purification are the breaking of carbon bonds and oxidation to carbon dioxide and water.
R3−C−0−CH。R3-C-0-CH.
1
(R+、Rt、Rsは飽和、不飽和のアルキル基)油に
熱をかけると脱水素とタール化が起こる。1 (R+, Rt, and Rs are saturated and unsaturated alkyl groups) When heat is applied to oil, dehydrogenation and tar formation occur.
タールを酸化分解するために450°C以上の高温が要
求される。High temperatures of 450°C or higher are required to oxidize and decompose tar.
そこで従来の多孔性被膜では上記熱分解の過程に触媒作
用を取り入れ比較的低温でタールを分解しようとするも
のである。Therefore, conventional porous coatings incorporate a catalytic action into the thermal decomposition process to decompose tar at a relatively low temperature.
しかし実用上、多孔性被膜は剥離しやすい、傷つきやす
い等の問題がある。また完全燃焼を目標とするとどうし
ても汚れの処理量の点で浄化能力に制限が出てくる。However, in practical use, porous coatings have problems such as being easily peeled off and easily damaged. Furthermore, if complete combustion is the goal, there will inevitably be a limit to the purification ability in terms of the amount of dirt that can be processed.
そこで本発明ではまず第1にタール成分と被膜表面との
結合力を弱めることに着眼した。Therefore, the present invention first focuses on weakening the bonding force between the tar component and the coating surface.
本発明でバインダーとして用いた半有機賞であるポリボ
ロシロキサン、ポリボロチタノシロキサンは450℃以
上で焼成すると無#9質化して非常に緻密な薄膜を形成
することができる。When the semi-organic polyborosiloxane and polyborotitanosiloxane used as the binder in the present invention are fired at 450° C. or higher, they become free of #9 and can form a very dense thin film.
例えば従来の多孔質被膜の場合には数十〜数百μレベル
の細孔を持っていたが、ポリボロシロキサン等をバイン
ダーとした前記薄膜の細孔は最高で数pレベルである。For example, conventional porous coatings have pores on the order of tens to hundreds of microns, but the pores of the thin film using polyborosiloxane or the like as a binder are at most on the order of several microns.
更に層状化合物を混入することにより被膜表面とタール
成分の離型性を上げた。Furthermore, by incorporating a layered compound, the releasability of the tar component from the coating surface was improved.
また第2に被膜の表層部分で油汚れを酸化分解させるこ
とに着眼し、触媒としてNiとMOの複合酸化物を混入
した。Second, we focused on oxidatively decomposing oil stains in the surface layer of the coating, and mixed a composite oxide of Ni and MO as a catalyst.
NiとMoの複合酸化物は石油やガソリン等の水素化分
解等に活性の高い触媒として知られている。A composite oxide of Ni and Mo is known as a highly active catalyst for hydrogenolysis of petroleum, gasoline, etc.
以上のように本発明の耐熱性被膜は、Ni−Mo複合酸
化物の酸化作用で油汚れを酸化分解し、更に被膜が緻密
で表面の滑り性がよいため焼は残ったタール成分や灰分
は簡単に剥離し、ふき取ることが可能であるため、オー
プン、グリル調理器庫内壁面に用いると、食品から飛散
して壁面に付着した油汚れは、熱をかけることにより浄
化することができる。As described above, the heat-resistant coating of the present invention oxidizes and decomposes oil stains due to the oxidizing action of the Ni-Mo composite oxide, and furthermore, since the coating is dense and has good surface slipperiness, the remaining tar components and ash are removed. Since it can be easily peeled off and wiped off, when used on the inner wall surface of an open or grill cooking appliance, oil stains scattered from food and attached to the wall surface can be cleaned by applying heat.
実施例 以下、本発明の一実施例について説明する。Example An embodiment of the present invention will be described below.
まず被膜の製法について説明する。First, the manufacturing method of the film will be explained.
バインダーとフィラー、層状化合物とNi。Binder and filler, layered compound and Ni.
Moの複合酸化物と溶剤を24時間、アトライタで分散
させ、できた塗料をスプレーガン(デビルビス製スプレ
ーガン、ノズルロ径1.4国φ、Air圧2〜2.5k
g/c+a)でステンレス(SO3304430〉基材
上に塗布しioo″C→500“01600°Cで順に
焼成して被膜を作成した。Mo complex oxide and solvent are dispersed in an attritor for 24 hours, and the resulting paint is sprayed with a spray gun (DeVilbiss spray gun, nozzle diameter 1.4 mm, air pressure 2 to 2.5 k).
g/c+a) onto a stainless steel (SO3304430> base material) and sequentially fired at 500°C to 1600°C to form a film.
NiMoの複合酸化物についてはNiは硝酸塩、Moは
アンモニウム塩を出発物質とし、各々の水溶液を混合し
生成した沈殿を濾過、水洗、乾燥、450°C焼戒した
ものを用いた。生成物の分析結果はNtO:MoO,ζ
35 : 36であった。For the NiMo composite oxide, starting materials were a nitrate for Ni and an ammonium salt for Mo, and the aqueous solutions of each were mixed, the resulting precipitate was filtered, washed with water, dried, and incinerated at 450°C. The analysis result of the product is NtO:MoO,ζ
It was 35:36.
次に被膜上に一定量のサラダ油を滴下し、一定温度に設
定したオーブン中に放置し、油の浄化テストを行った。Next, a certain amount of salad oil was dropped onto the film, and the film was left in an oven set at a certain temperature to conduct an oil purification test.
被膜を形成するための塗料の配合及び油の浄化テスト結
果をまとめ次表に示した。The formulation of the paint used to form the film and the results of the oil purification test are summarized in the table below.
配合はすべて重量比で示した。All formulations are shown in weight ratios.
以下余白
油浄化テストは380’Cで行い、浄化に要した時間を
示した。Mo St 、WSz 、BNを添加し、バイ
ンダーとしてポリボロシロキサンあるいはポリチタノシ
ロキサンを用いたNα■〜恥■の膜は滑り性がよく、N
[l[相]、 No■の膜は多孔質に仕上がっていた。The margin oil purification test below was conducted at 380'C, and the time required for purification is shown. The films of Nα■ to Shai■ containing Mo St, WSz, and BN and using polyborosiloxane or polytitanosiloxane as a binder have good slipperiness, and
[l [phase], No. 2 membrane was porous.
MoS2.WS、、BNの中ではMoS、を添加した膜
が鉛筆硬度9Hと非常に高い硬度を示した。MoS2. Among WS and BN, the film containing MoS had a very high pencil hardness of 9H.
次にMoS、と酸化触媒の添加を検討した。Nα■、N
α■、Nα■に結果を示す。Nα■のように通常の油分
解に用いられるCuMnOxのような遷移金属の酸化物
は、膜が緻密で酸素拡散が悪く、油を燃焼させることが
できないため浄化性能が悪い。Next, we investigated the addition of MoS and an oxidation catalyst. Nα■, N
The results are shown in α■ and Nα■. Transition metal oxides such as CuMnOx, which are commonly used in oil decomposition, such as Nα■, have dense membranes and poor oxygen diffusion, making it impossible to combust oil, resulting in poor purification performance.
また金属酸化物の還元による塗膜の変色が目立った。N
α■のように希土類の酸化物であるC e Otを加え
ると油浄化性能は高いが膜表面に黄色く照りのある変色
が残った。In addition, discoloration of the coating film due to reduction of metal oxides was noticeable. N
When C e Ot, which is a rare earth oxide like α■, is added, the oil purification performance is high, but a yellow and shiny discoloration remains on the membrane surface.
Nα■に示すようにN i OM o O3を添加した
場合には浄化性能も高く塗膜の変色もほとんどなかった
。NtO−MoO,は遷移金属の酸化物のように還元に
よる変色はおこらず、被膜の表層部で油汚れの脱水素や
分解がおこなわれていると考えられる。As shown in Nα■, when N i OMo O3 was added, the purification performance was high and there was almost no discoloration of the coating film. Unlike transition metal oxides, NtO-MoO does not change color due to reduction, and it is thought that dehydrogenation and decomposition of oil stains occur in the surface layer of the coating.
以上の結果からMob、とNtO−MoO,を添加し、
更に黒色顔料としてFe、○、・CuO・MnxO3を
少量加えたNα■の膜が硬度、浄化性能共に最も優れて
いることがわかった。From the above results, we added Mob and NtO-MoO,
Furthermore, it was found that a film of Nα■ to which a small amount of Fe, ○, .CuO.MnxO3 was added as a black pigment was the most excellent in both hardness and purification performance.
尚、Alz○、は充填剤の総量をそろえるために添加し
たものであり、またバインダーだけをポリボロシロキサ
ンからポリチタノシロキサンに変えた場合や両者の混合
の場合も物性、浄化能力に影響がないことが阻■、Nα
■よりわかった。Note that Alz○ is added to equalize the total amount of fillers, and changing only the binder from polyborosiloxane to polytitanosiloxane or mixing the two will affect the physical properties and purification ability. Not having it is a hindrance, Nα
■I understand more.
またリン酸塩やケイ酸塩をバインダーとして用いた阻[
相]、阻■は膜のPHが酸あるいはアルカリに片寄るた
めの油の浄化性能が悪く、多孔質であるためタール分が
多孔質内にも沈着していた。Also, inhibitors using phosphates or silicates as binders [
In phase 1 and 2, the PH of the membrane was biased toward acid or alkali, resulting in poor oil purification performance, and since the membrane was porous, tar was deposited within the pores.
以上のように本発明の耐熱性被膜は、油汚れを脱水素及
び分解し、更に被膜表面とタールとの結合力を弱めるこ
とができるため調理器庫内壁面の実用に適した耐熱性被
膜である。As described above, the heat-resistant coating of the present invention can dehydrogenate and decompose oil stains, and further weaken the binding force between the coating surface and tar, making it a heat-resistant coating suitable for practical use on the inner wall surface of a cooking appliance. be.
発明の詳細
な説明したように本発明の耐熱性被膜は、硬度が高く、
表面の滑り性が良好であり、更に油汚れの分解作用を持
っているため調理器庫内の汚れ浄化に優れた被膜を得る
ことが可能である。As described in the detailed description of the invention, the heat-resistant coating of the present invention has high hardness,
It has good surface slipperiness and also has the ability to decompose oil stains, making it possible to obtain a coating that is excellent in cleaning stains inside the cooking appliance.
調理器庫内壁に塗布し、被膜に汚れが付着した後で被膜
を加熱することで汚れがなくなり、また焼は残った灰分
や付着物等は簡単にはがれふき取ることができるため、
調理器庫内壁をいつまでもきれいな状態に保つことがで
きる。By applying it to the inner wall of the cooking appliance and heating the coating after it becomes dirty, the dirt will disappear, and the remaining ash and deposits can be easily peeled off and wiped off.
The inner walls of the cooking cabinet can be kept clean forever.
Claims (2)
サンないし前記2種の混合物をバインダーとし、層状構
造を持つ化合物とNi、Moの複合酸化物、更に必要に
応じてホーロー成分やガラス粉末を含んだ耐熱性被膜。(1) A heat-resistant material containing polyborosiloxane, polyborotitanosiloxane, or a mixture of the two mentioned above as a binder, a compound with a layered structure, a composite oxide of Ni and Mo, and optionally an enamel component or glass powder. sex capsule.
サンないし前記2種の混合物をバインダーとし、層状構
造を持つ化合物とNi、Moの複合酸化物、更に必要に
応じてホーロー成分やガラス粉末を含んだ耐熱性被膜と
調理用調理室内壁に前記耐熱性被膜を塗布し、前記調理
室を加熱するヒータを有する耐熱性被膜を施した加熱調
理器。(2) A heat-resistant product containing polyborosiloxane, polyborotitanosiloxane, or a mixture of the two mentioned above as a binder, a compound with a layered structure, a composite oxide of Ni and Mo, and optionally an enamel component or glass powder. The heat-resistant coating is coated on the heat-resistant coating and the inner wall of the cooking chamber, and the heat-resistant coating is provided with a heater for heating the cooking chamber.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17954189A JPH0343474A (en) | 1989-07-11 | 1989-07-11 | Heat-resistant coating film and heating cooker coated with the same film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17954189A JPH0343474A (en) | 1989-07-11 | 1989-07-11 | Heat-resistant coating film and heating cooker coated with the same film |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH0343474A true JPH0343474A (en) | 1991-02-25 |
Family
ID=16067556
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17954189A Pending JPH0343474A (en) | 1989-07-11 | 1989-07-11 | Heat-resistant coating film and heating cooker coated with the same film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0343474A (en) |
-
1989
- 1989-07-11 JP JP17954189A patent/JPH0343474A/en active Pending
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