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JPS6215109B2 - - Google Patents
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JPS6215109B2 - - Google Patents

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Publication number
JPS6215109B2
JPS6215109B2 JP54114816A JP11481679A JPS6215109B2 JP S6215109 B2 JPS6215109 B2 JP S6215109B2 JP 54114816 A JP54114816 A JP 54114816A JP 11481679 A JP11481679 A JP 11481679A JP S6215109 B2 JPS6215109 B2 JP S6215109B2
Authority
JP
Japan
Prior art keywords
oils
fats
film
polymerization
self
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
Application number
JP54114816A
Other languages
Japanese (ja)
Other versions
JPS55155065A (en
Inventor
Eiji Kusaki
Tomio Izumioka
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Consejo Superior de Investigaciones Cientificas CSIC
Mie Yushikako KK
Original Assignee
Consejo Superior de Investigaciones Cientificas CSIC
Mie Yushikako KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Consejo Superior de Investigaciones Cientificas CSIC, Mie Yushikako KK filed Critical Consejo Superior de Investigaciones Cientificas CSIC
Priority to JP11481679A priority Critical patent/JPS55155065A/en
Publication of JPS55155065A publication Critical patent/JPS55155065A/en
Publication of JPS6215109B2 publication Critical patent/JPS6215109B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は調理装置におけるオーブンの壁面に塗
布して自己浄化型被覆層を形成するためのセルフ
クリーニング用塗料に係る。 オーブン等の調理装置の内壁面は食品より飛散
する物質で汚染されて異臭をはなつたり、酸化変
色して不快感を与えている。さらにオーブン内壁
面に付着した油脂類は加熱されると酸化変色して
重合物となり強力な密着力を持つ固化皮膜となり
除去、清掃がきわめて困難となる。 最近では、酸化触媒を混入した多孔質皮膜をオ
ーブンの内壁面に施こして、酸化触媒効果によつ
て分解し除去しようとする調理装置のある。しか
し電気オーブンの実調理時は庫内壁温度が200℃
を越えることは少ないため、触媒作用が活発に働
く温度(MnO2の場合250℃前後)に達しないこ
とが多く、自己浄化型被覆層に付着した油脂類は
時間の経過とともに油脂の重合が進み、油脂類の
重合膜が触媒を被つて触媒性能を低下させたり、
これらがくりかえされると最後には触媒作用がな
くなり、油脂類は多孔質層の孔などに入り込んで
固化してしまい除去することが更に困難になつて
いる。 本発明はこのような油脂類の重合皮膜による壁
面汚染を少なくするためのセルフクリーニング用
塗料に係り、セルフクリーニング用皮膜として酸
化触媒作用を有する物質と、重合阻止作用を有す
る物質を併用し耐熱造膜組成物で多孔質粗面層に
仕上げることを特徴とする。 壁面に付着する動物性、及び植物性油脂類は加
熱されると蒸発、重合、炭化分解などの現象が起
きる。この現象は温度、時間、昇温、速度などに
関係していて、200℃以下では蒸発、炭化、分解
が少なく重合が激しくなる。250℃以上では蒸
発、炭化、分解、重合が同時におこなわれ、油脂
類の重合物は炭化され焼結する。 電気オーブンやオーブンレンジの壁面温度は、
300℃以上に達することは少なく、達しても局部
的である。いずれにしても300℃以下の温度条件
においては油脂類の重合物及び炭化物が多く生成
した汚染の原因となる。殊に、酸化触媒単独を含
有した皮膜に付着した油脂類は、200℃以下にお
いて重合作用が働き重合皮膜を多く生成し逆に除
去作業を困難にしている。 このような点に着目し、調理装置のオーブン壁
に最適で、比較的低温でもセルフクリーニング効
果の良い塗料およびセルフクリーニング皮膜を開
発するため、次のような実験を行ない、油脂類に
対し有効な成分を選別した。 〔実験方法〕 混合油(バター10%、コーン油20%、魚油10
%、牛肉脂肪20%、ナタネ油20%、大豆油20%)
6重量部と選別しようとする物質(前もつて500
℃、1時間の加熱処理をしておく)4重量部を練
り合わせて耐熱ガラス表面にアプリケータにて30
ミクロンの厚さにひろげ、そして200℃で20分間
加熱した後その表面状態を判定し、さらに250℃
で1時間加熱した後もう一度その表面状態を判定
する。 〔判定基準〕 イ 250℃、1時間加熱後の混合油の蒸発率を調
べる。 蒸発率=減少した重量/用いた混合油の重量×100 蒸発率が100%越えるものは選別しようとす
る物質の酸素等が飛散したためである。 蒸発率の値が小さいことは混合油があまり蒸
発しなかつたことを意味する。 ロ 実験材料の表面状態を観察し、どのような作
用を有するかを次の第1表の基準表で判定し、
各実験材料ごとA、B、C、Dのランク付けを
する。
The present invention relates to a self-cleaning paint that is applied to the wall surface of an oven in a cooking device to form a self-cleaning coating layer. The inner walls of cooking devices such as ovens are contaminated with substances scattered from food, giving off unpleasant odors and discoloring due to oxidation, giving an unpleasant feeling. Furthermore, when heated, oils and fats adhering to the inner wall surface of the oven undergo oxidative discoloration and turn into polymers, forming a solidified film with strong adhesion that is extremely difficult to remove and clean. Recently, there is a cooking device in which a porous film containing an oxidation catalyst is applied to the inner wall surface of the oven, and the porous film is decomposed and removed by the oxidation catalyst effect. However, when actually cooking in an electric oven, the internal wall temperature is 200℃.
Because the temperature rarely exceeds 100°F, it often does not reach the temperature at which the catalytic action is active (around 250°C in the case of MnO 2 ), and the oils and fats that adhere to the self-purifying coating layer will polymerize over time. , a polymer film of oils and fats may cover the catalyst and reduce catalyst performance,
When these processes are repeated, the catalytic action eventually disappears, and the fats and oils enter the pores of the porous layer and solidify, making it even more difficult to remove them. The present invention relates to a self-cleaning paint for reducing wall surface contamination caused by such a polymerized film of oils and fats. It is characterized by finishing a porous rough surface layer with a membrane composition. When animal and vegetable oils and fats that adhere to walls are heated, phenomena such as evaporation, polymerization, and carbonization occur. This phenomenon is related to temperature, time, temperature rise, speed, etc. Below 200℃, there is little evaporation, carbonization, and decomposition, and polymerization becomes more intense. At temperatures above 250°C, evaporation, carbonization, decomposition, and polymerization occur simultaneously, and the polymerized oils and fats are carbonized and sintered. The wall temperature of an electric oven or oven range is
Temperatures rarely reach 300°C or higher, and even if they do, they are localized. In any case, if the temperature is below 300°C, a large amount of polymerized and charred substances of oils and fats will be produced, causing contamination. In particular, oils and fats adhering to a film containing only an oxidation catalyst undergo polymerization at temperatures below 200°C, producing a large amount of polymerized film, making removal work difficult. Focusing on these points, we conducted the following experiments to develop paints and self-cleaning films that are ideal for the oven walls of cooking equipment and have good self-cleaning effects even at relatively low temperatures. Ingredients were selected. [Experiment method] Mixed oil (10% butter, 20% corn oil, 10% fish oil)
%, beef fat 20%, rapeseed oil 20%, soybean oil 20%)
6 parts by weight and the substance to be sorted (previously 500 parts by weight)
℃, 1 hour heat treatment)) Mix together 4 parts by weight and apply to the surface of heat-resistant glass using an applicator for 30 minutes.
After spreading to a micron thickness and heating at 200℃ for 20 minutes, the surface condition was determined, and then heated to 250℃.
After heating for 1 hour, the surface condition was determined again. [Judgment Criteria] A. Check the evaporation rate of the mixed oil after heating at 250℃ for 1 hour. Evaporation rate = weight decreased / weight of mixed oil used × 100 If the evaporation rate exceeds 100%, it is because oxygen, etc. of the substance to be sorted has dispersed. A small value of evaporation rate means that the mixed oil did not evaporate much. (b) Observe the surface condition of the experimental material and judge what kind of effect it has using the standard table in Table 1 below.
Rank each experimental material as A, B, C, or D.

〔実験結果〕〔Experimental result〕

上記実験方法、判定基準に基づき種々の物質に
ついて実験した結果、第2表のようなデータが得
られた。
As a result of experiments on various substances based on the above experimental method and criteria, data as shown in Table 2 was obtained.

【表】【table】

【表】 第2表のデータから作用について分類すると次
のようになる。 イ 酸化分解作用を有する物質 …酸化マンガン、酸化ニツケル、白金、パラジ
ウム、その他 ロ 重合阻止作用を有する物質 …酸化アンチモン、水酸化アルミニウム、リン
酸系フリツトフリツト、アンチモン粉末、その
他 ハ 重合促進作用を有する物質 …酸化鉛、酸化亜鉛、鉛ガラス、酸化コバル
ト、その他 ニ いずれの作用も有しない物質 …硅石粉、酸化チタン、炭酸カルシウム、マイ
カー粉、その他 第2表において、蒸発率が小さく且つ重合阻止
作用を示す物質が低温にて油脂類の重合化を阻止
する効果がある。このうち、セルフクリーニング
用塗料の成分として、コスト、塗膜の密着性、多
孔質形成効果などを考慮すると、水酸化アルミニ
ウム、酸化アンチモン、リン酸系フリツト又はこ
れらの混合物が重合阻止剤に最適である。 また、そのセルフクリーニング用塗料に含まれ
る酸化触媒としては、白金、パラジウム等の貴金
属もしくは酸化マンガン、酸化ニツケル等の金属
酸化物が有効で、単独或いは混合して用いること
が出来る。 前記実験結果よつて判明したことは次の点であ
る。重合促進作用を有する物質いわゆる重合固
化触媒と油脂類とが接触すると、低温でしかも早
く固化皮膜を形成し油脂類の蒸発、分解を著しく
低下させることにより自己浄化型被覆層に使用す
べきではない。逆に重合阻止作用を有する物質
を多孔質層に分散させることによつて油脂類の通
常の加熱重合を阻止すると共に重合触媒の触媒毒
として働き固化皮膜の生成を抑制することが明ら
かとなつた。重合阻止作用を有する物質と酸化
触媒とを併用して油脂類の重合を阻止すれば混合
油の一部が低分子化された蒸発効果が活発になり
多量の混合油を短時間でガス化することが可能と
なりさらに低温(50℃前後)時の蒸発も可能とな
つた。 重合阻止によつて蒸発をさらに助ける条件とし
て、多孔粗面と重合阻止作用を有する物質の表面
積及び油脂類との接触の状態と距離等がある。最
も効果的な条件は油脂類が作用を受ける距離、す
なわち半径15ミクロン以内に作用を有する物質が
存在していければならない。それには油類を皮膜
中に浸透させる表面にひろげるか又は両者を同時
に有することが必要である。油脂類を浸透及び横
ひろがりを速くさせる為には皮膜を点状、線状又
は点状、線状同時に有する多孔質で粗面な仕上り
とすればよく、それによつて15ミクロン以内に油
脂類をひろげることができる。油脂類を誘導する
のは粒子の重なり、突起でできた孔でありその壁
面に出来る突起である。更には重合阻止作用が効
果的であるためには重合阻止作用を有する物質の
表面は露出し、この油脂類と接触していなければ
ならない。 次に、本発明の塗料を用いてセルフクリーニン
グ用皮膜を形成する多孔質粗面被覆層の製造法に
付いて一実施例により説明する。 まず、酸化作用を有する酸化マンガンと酸化ニ
ツケルをボールミルで50ミクロン以下の粒子に粉
砕し、重合阻止作用を有する水酸化アルミニウム
の多角板状結晶と、リン酸系フリツト及び多角形
でしかも50ミクロン以下の表面に凹凸のある硅石
粉をエポキシ変性シリコーン樹脂初期重合物のキ
シレン溶液に撹拌機で分散して、シンナーで粘度
をチクソトロピー状に調整し塗料(セルフクリー
ニング用塗料という。)とする。この塗料を撹拌
機付圧槽タンクに入れ0.5〜1.5Kg/cm2の圧力をか
けて口径1mm以上の吹付用ガンで2〜4Kg/cm2
エアー圧により噴化して被塗装物に塗布する。塗
布皮膜は複数回塗布を繰返して乾燥皮膜が150ミ
クロン以上〜300ミクロン以下になるように塗布
して、常温で10分間放置後、200℃で5分間加熱
して有機溶剤を完全に揮発させて、更に530℃で
10分間焼成後、冷却し塗膜の成形が完了する。
尚、実施例として使用された塗料の成分は第3表
の通りである。
[Table] Based on the data in Table 2, the effects are classified as follows. (a) Substances that have oxidative decomposition effects: manganese oxide, nickel oxide, platinum, palladium, and others; (b) Substances that inhibit polymerization: antimony oxide, aluminum hydroxide, phosphoric acid frits, antimony powder, and others (c) Substances that promote polymerization. ...Lead oxide, zinc oxide, lead glass, cobalt oxide, and other substances that do not have any of the following effects...silica powder, titanium oxide, calcium carbonate, mica powder, etc. In Table 2, substances that have a low evaporation rate and have a polymerization inhibiting effect The substance shown has the effect of inhibiting the polymerization of oils and fats at low temperatures. Among these, aluminum hydroxide, antimony oxide, phosphoric acid frit, or a mixture thereof are most suitable as polymerization inhibitors as components of self-cleaning paints, considering cost, adhesion of the paint film, porosity formation effect, etc. be. Further, as the oxidation catalyst contained in the self-cleaning paint, noble metals such as platinum and palladium, or metal oxides such as manganese oxide and nickel oxide are effective, and they can be used alone or in combination. The following points were found from the above experimental results. When oils and fats come into contact with substances that have a polymerization-promoting effect, so-called polymerization solidification catalysts, they form a solidified film quickly at low temperatures, significantly reducing the evaporation and decomposition of oils and fats, so they should not be used in self-purifying coating layers. . On the contrary, it has become clear that by dispersing a substance that has a polymerization inhibiting effect in a porous layer, it can inhibit the normal thermal polymerization of oils and fats, and also act as a catalyst poison for the polymerization catalyst, suppressing the formation of a solidified film. . If the polymerization of oils and fats is inhibited by using a substance that has a polymerization inhibiting effect in combination with an oxidation catalyst, the evaporation effect in which part of the mixed oil is reduced to low molecular weight becomes active, and a large amount of the mixed oil can be gasified in a short time. This also made it possible to evaporate at low temperatures (around 50℃). Conditions that further assist evaporation by inhibiting polymerization include the surface area of the porous rough surface and the substance having a polymerization inhibiting effect, and the state and distance of contact with the oil and fat. The most effective condition is that a substance that has an effect must exist within a radius of 15 microns, which is the distance at which oils and fats are affected. This requires the presence of oils on the surface that penetrate into the film, or both at the same time. In order to speed up the penetration and lateral spread of oils and fats, the film should have a porous and rough finish that is dotted, linear, or dotted and linear at the same time. It can be expanded. What guides fats and oils are the overlapping particles and pores formed by protrusions, and the protrusions formed on the walls of these pores. Furthermore, in order for the polymerization inhibiting action to be effective, the surface of the substance having the polymerization inhibiting action must be exposed and in contact with the oils and fats. Next, a method for manufacturing a porous rough surface coating layer forming a self-cleaning film using the coating material of the present invention will be described with reference to an example. First, manganese oxide and nickel oxide, which have an oxidizing effect, are ground into particles of 50 microns or less using a ball mill, and polygonal plate-shaped crystals of aluminum hydroxide, which has a polymerization-inhibiting effect, a phosphoric acid frit, and polygonal particles of 50 microns or less are produced. The silica powder, which has an uneven surface, is dispersed in a xylene solution of the initial polymerization of epoxy-modified silicone resin using a stirrer, and the viscosity is adjusted to a thixotropic state using thinner to form a paint (referred to as a self-cleaning paint). This paint is placed in a pressure tank with an agitator and a pressure of 0.5 to 1.5 kg/cm 2 is applied, and a spray gun with a diameter of 1 mm or more is used to atomize it with air pressure of 2 to 4 kg/cm 2 and applied to the object to be painted. . The coated film is applied multiple times until the dry film is 150 microns or more and 300 microns or less, left at room temperature for 10 minutes, and then heated at 200°C for 5 minutes to completely volatilize the organic solvent. , further at 530℃
After baking for 10 minutes, it is cooled and the coating is completed.
The components of the paints used in the examples are shown in Table 3.

【表】 前記実施例に用いる酸化触媒、重合阻止剤、助
剤の粒径、形状及びその表面粗度は電子顕微鏡写
真第1図a,b,c,d,e,f,g,h,i,
jに示した状態であり、硬化皮膜の断面は電子顕
微鏡写真第2図のように硅石粉と水酸アルミニウ
ム及びリン酸系フリツト、酸化マンガンの粗粒子
をシリコン樹脂の分解物で結合して造膜組成の骨
核をなし孔及び粗面を構成している。この孔の壁
は、更に凹凸があり油脂類をひろげる役割を果し
ている。油脂類のこの孔への浸透速度は早いほう
が良い。それは重合阻止作用の効果は受けにくい
表面では15ミクロンの厚さの油膜が重合阻止作用
を受ける限界で、それ以上になると加熱によつて
重合固化被膜を形成する。油脂類の塗膜への浸透
速度は皮膜表面に4〜5mgのサラダ油を滴下し、
25℃の雰囲気中で油にによる光沢がなくなるまで
の時間が15分以内であれば、加熱されても表面に
重合皮膜を生成しない。 実施例によつて得られたセルフクリーニング用
皮膜を形成する多孔質被覆層の油脂類の蒸発分解
効果を確認するためには熱天秤を用いて測定を行
うが、測定方法を説明すると、まず基材に結合さ
れた多孔質層片を直径7mmの円試片に仕上げ、熱
天秤の白金容器の中に上向けに入れて5mgのサラ
ダ油を滴下して1分以内に加熱を開始する。ここ
で、常温から300℃まで20℃/分の速度で昇温し
たときの各温度でのオイルの減量を測定した結果
を第5図aで表わしている。これによれば減量の
開始温度は低温で始まるほど有効でありアルミ
板、市販セルフクリーニングホーロー(以後既存
SCとする。)が200℃前後で減量が始つているの
に対して本発明の皮膜では50℃前後より減量が始
まつており低温時の性能がすぐれているのがわか
る。 第5図b,cは熱天秤の温度を200℃、250℃に
保温した時のサラダ油の減量を表わしたものであ
り200℃においてはアルミ板と既存SCとの差がほ
とんどなく既存SCはほとんどその効果を有して
いない。250℃においてもアルミ板に比べて既存
SCの効果は確認されるが、いずれの温度におい
ても本発明による皮膜が示す減量には及ばないこ
とが明らかである。さらに実際の加熱装置等で壁
面の汚染を比較するとその差は更に拡大評価の対
象となる。尚、実施例に使用した結合剤はシリコ
ーン系樹脂であるが、リン酸塩又はホーローフリ
ツトであつても効果は変らないものの電子顕微鏡
写真第3図a,b,cの既存SCの面のように、
触媒がホーローユウ薬にとけ込み多孔度は荒く粒
子表面は平滑であつてはならない。 本発明は先に述べた酸化触媒と、重合阻止剤を
併用しその作用を有する粒子又は増量粉体粒子又
は混合粒子の粒径及び形状とその表面粗度の重な
りによつて形成する特有の皮膜が蒸発効果を助け
ており、本発明の塗料に負うところの皮膜表面の
電子顕微鏡写真第4図a,b,cのように、処方
で用いた水酸化アルミニウム、硅石粉、リン酸系
フリツト、等の5〜50ミクロン級の粒子を骨核に
して、その粒子表面がもつて凹凸及び酸化ニツケ
ル、酸化マンガン等の酸化触媒の微粒子が付着し
てできる凹凸の表面積は油脂類のひろがりを助
け、接触面積を増すと同時に蒸発面をも増すこと
の出来る状態でなければならない。 本発明の塗料に負うところの皮膜によるサラダ
油の減量は分解か、又は蒸発によるものかを明ら
かにするため炉中で発生したガスをガスクロマト
グラフイに通して分析を行つた。その結果、水、
炭酸ガス等の成分が確認された。250以下での減
量は大半が油脂類の蒸発物であることが明らかに
なつた。しかしアルミニウム板から蒸発した成分
と、本発明塗料による皮膜より蒸発した成分は異
なり、ほとんどが低沸点物に分解されて蒸発して
いる。又本発明塗料による皮膜中に残留したわず
かなタール状物質を再度300℃で加熱した時、
水、炭酸ガスが多量に発生した。このことは本発
明塗料による皮膜では油脂類が重合化していない
事を示す。尚、本発明塗料よつて得られた皮膜を
電気オーブン等の調理装置にもちいると壁面に付
着した油脂類は調理中だけでなく調理が終了した
後壁面が自然冷却されていく間にも効果が発揮さ
れる。 以上に説明したように、この発明塗料によれば
酸化触媒と重合阻止剤を併用して多孔質粗面のセ
ルフクリーニング用皮膜を壁面に形成することに
より比較的低温で油脂類の蒸発、分解を効率良く
行なうことができる。すなわち、重合阻止剤によ
つて油脂類の重合反応が阻止されて長時間流動性
を示すため、酸化触媒粒子面に油脂類が広がつた
り対流が起こり、全体的に触媒の影響を受け易
く、一部に低分子化するものも含めて蒸発効果を
高めることになり、粗面から大量の油脂類が低温
でしかも早く、大気中に蒸発させることができ
る。又、少量の重合皮膜が生成しても、皮膜が薄
く酸化触媒効果の活発な位置にあり容易に分解す
ることができる。このような酸化触媒と重合阻止
剤を併用した多孔質粗面は、油脂類の発生する調
理装置の壁面、特に天面や排気ダクトに使用すれ
ば最適である。
[Table] The particle size, shape, and surface roughness of the oxidation catalyst, polymerization inhibitor, and auxiliary agent used in the above examples are shown in electron micrographs (a, b, c, d, e, f, g, h, i,
The cross section of the cured film is as shown in Figure 2, an electron micrograph, and is made by bonding silica powder, aluminum hydroxide, phosphate frits, and coarse particles of manganese oxide with a decomposed product of silicone resin. It has a bone core with membranous composition and constitutes pores and rough surfaces. The walls of this hole are also uneven and play a role in spreading oils and fats. The faster the rate of penetration of oils and fats into these pores, the better. On surfaces that are less susceptible to polymerization inhibiting effects, an oil film of 15 microns in thickness is the limit at which polymerization inhibiting effects occur, and beyond this, a polymerized and solidified film is formed by heating. The penetration rate of oils and fats into the coating film can be determined by dropping 4 to 5 mg of salad oil onto the coating surface.
If it takes less than 15 minutes for the luster caused by oil to disappear in an atmosphere of 25°C, a polymeric film will not form on the surface even if heated. In order to confirm the evaporative decomposition effect of oils and fats in the porous coating layer forming the self-cleaning film obtained in the example, a thermobalance is used to perform measurement. The porous layer piece bonded to the material is finished into a circular piece with a diameter of 7 mm, placed face up in a platinum container of a thermobalance, and 5 mg of salad oil is added dropwise to start heating within 1 minute. Here, the results of measuring the weight loss of oil at each temperature when the temperature was raised from room temperature to 300°C at a rate of 20°C/min are shown in Figure 5a. According to this, the lower the starting temperature for weight loss, the more effective it is.
It shall be SC. ) starts to lose weight at around 200°C, while the film of the present invention starts to lose weight at around 50°C, demonstrating its excellent performance at low temperatures. Figures b and c in Figure 5 show the loss of salad oil when the temperature of the thermobalance is kept at 200℃ and 250℃.At 200℃, there is almost no difference between the aluminum plate and the existing SC. It doesn't have that effect. Compared to aluminum plate, even at 250℃
Although the effect of SC is confirmed, it is clear that it does not reach the weight loss exhibited by the coating according to the present invention at any temperature. Furthermore, when comparing wall contamination with actual heating equipment, etc., the difference becomes the subject of further expanded evaluation. Although the binder used in the examples is a silicone resin, the effect remains the same even if it is a phosphate or hollow frit. like,
The catalyst must be dissolved in the enamel, and the porosity must be rough and the particle surface must not be smooth. The present invention uses the above-mentioned oxidation catalyst in combination with a polymerization inhibitor to form a unique film formed by the overlap of the particle size and shape of particles having the effect, expanded powder particles, or mixed particles and their surface roughness. The aluminum hydroxide, silica powder, phosphoric acid frits, and The roughness of the particle surface and the surface area of the unevenness created by the adhesion of fine particles of oxidation catalysts such as nickel oxide and manganese oxide help the spread of oils and fats. It must be possible to increase the contact area and at the same time increase the evaporation surface. In order to clarify whether the loss of salad oil due to the film caused by the coating of the present invention was due to decomposition or evaporation, the gas generated in the furnace was analyzed by gas chromatography. As a result, water,
Components such as carbon dioxide gas were confirmed. It became clear that most of the weight loss below 250 was due to evaporation of fats and oils. However, the components that evaporated from the aluminum plate and the components that evaporated from the film formed by the paint of the present invention are different, and most of them are decomposed into low boiling point substances and evaporated. Also, when the slight tar-like substance remaining in the film formed by the paint of the present invention was heated again at 300℃,
Large amounts of water and carbon dioxide gas were generated. This indicates that oils and fats are not polymerized in the film formed by the paint of the present invention. Furthermore, when the film obtained by the paint of the present invention is used in a cooking device such as an electric oven, fats and oils adhering to the wall surface will be effectively removed not only during cooking but also while the wall surface naturally cools down after cooking is completed. is demonstrated. As explained above, the inventive paint uses an oxidation catalyst and a polymerization inhibitor in combination to form a porous, rough self-cleaning film on the wall surface, thereby preventing the evaporation and decomposition of oils and fats at relatively low temperatures. It can be done efficiently. In other words, the polymerization reaction of the oils and fats is inhibited by the polymerization inhibitor and the oils and fats exhibit fluidity for a long time, so the oils and fats spread on the oxidation catalyst particle surface and convection occurs, making the whole particle susceptible to the influence of the catalyst. This increases the evaporation effect, including some of the substances that become low in molecular weight, allowing large amounts of fats and oils to evaporate into the atmosphere at low temperatures and quickly from the rough surface. Furthermore, even if a small amount of polymeric film is formed, the film is thin and located at a position where the oxidation catalyst effect is active and can be easily decomposed. Such a porous rough surface using a combination of an oxidation catalyst and a polymerization inhibitor is optimal if used on the wall surface of a cooking device where fats and oils are generated, especially on the top surface and exhaust duct.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図a,bは倍率40倍、900倍による本発明
のセルフクリーニング用皮膜に分散させる水酸化
アルミニウムの表面状態を示す図、第1図c,d
は同様に倍率100倍、1700倍によるリン酸系フリ
ツトの表面状態を示す図、第1図e,fは同様に
倍率300倍、4000倍による硅石粉の表面状態を示
す図、第1図g,hは同様に倍率100倍、1700倍
による酸化ニツケルの表面状態を示す図、第1図
i,jは同様に倍率100倍、220倍による酸化マン
ガンの表面状態を示す図。第2図は本発明皮膜の
倍率700倍による断面粒子配列を示す図。第3図
a,b,cは従来の各種セルフクリーニング用皮
膜表面の状態を示す倍率100倍、300倍、2600倍に
よる図。第4図a,b,cは本発明によるセルフ
クリーニング用皮膜表面の状態を示す倍率100
倍、600倍、2700倍による図である。第5図aは
温度上昇に対するサラダ油の減量を示す図、第5
図bは200℃におけるサラダ油減量の時間変化を
示す図、第5図cは同250℃におけるサラダ油減
量の時間変化を示す図である。 ただし、●―●は本発明の実施例、×―×は既
存S・C、〇―〇はアルミ板の特性を示す。
Figures 1a and b are views showing the surface condition of aluminum hydroxide dispersed in the self-cleaning film of the present invention at magnifications of 40x and 900x, Figures 1c and d
Similarly, Figure 1 e and f are diagrams showing the surface condition of silica powder at 300 and 4000 times magnification, Figure 1 g , h are diagrams showing the surface state of nickel oxide at 100x and 1700x magnification, and Figures i and j are diagrams showing the surface state of manganese oxide at 100x and 220x magnification. FIG. 2 is a diagram showing the cross-sectional particle arrangement of the film of the present invention at a magnification of 700 times. Figures 3a, b, and c are diagrams showing the surface conditions of various conventional self-cleaning films at magnifications of 100x, 300x, and 2600x. Figures 4a, b, and c show the state of the surface of the self-cleaning film according to the present invention at a magnification of 100.
The figures are magnified by magnification, 600x, and 2700x. Figure 5a is a diagram showing the loss of salad oil with respect to temperature rise.
Figure b is a graph showing the time change in the weight loss of salad oil at 200°C, and Figure 5c is a view showing the time change in the weight loss of salad oil at 250°C. However, ●--● are examples of the present invention, ×--× are existing S/C, and 〇-〇 are the characteristics of the aluminum plate.

Claims (1)

【特許請求の範囲】[Claims] 1 耐熱造膜組成物に酸化触媒作用を有する金属
若しくは金属酸化物又はそれらの混合物とを含有
してなるセルフクリーニング用塗料において、水
酸化アルミニウム、酸化アンチモン、リン酸フリ
ツト又はそれらの混合物から選ばれた重合阻止剤
を混合したセルフクリーニング用塗料。
1. A self-cleaning paint comprising a heat-resistant film-forming composition containing a metal or metal oxide having an oxidation catalytic action, or a mixture thereof, which is selected from aluminum hydroxide, antimony oxide, phosphoric acid frit, or a mixture thereof. A self-cleaning paint containing a polymerization inhibitor.
JP11481679A 1979-09-06 1979-09-06 Self-cleaning paint Granted JPS55155065A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11481679A JPS55155065A (en) 1979-09-06 1979-09-06 Self-cleaning paint

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11481679A JPS55155065A (en) 1979-09-06 1979-09-06 Self-cleaning paint

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP6485179A Division JPS55155738A (en) 1979-05-24 1979-05-24 Film for self-cleaning and its production

Publications (2)

Publication Number Publication Date
JPS55155065A JPS55155065A (en) 1980-12-03
JPS6215109B2 true JPS6215109B2 (en) 1987-04-06

Family

ID=14647395

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11481679A Granted JPS55155065A (en) 1979-09-06 1979-09-06 Self-cleaning paint

Country Status (1)

Country Link
JP (1) JPS55155065A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01167379A (en) * 1987-12-23 1989-07-03 Sharp Corp Self-cleaning film material

Also Published As

Publication number Publication date
JPS55155065A (en) 1980-12-03

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