JPH0556855A - Cooker - Google Patents

Cooker

Info

Publication number
JPH0556855A
JPH0556855A JP21946691A JP21946691A JPH0556855A JP H0556855 A JPH0556855 A JP H0556855A JP 21946691 A JP21946691 A JP 21946691A JP 21946691 A JP21946691 A JP 21946691A JP H0556855 A JPH0556855 A JP H0556855A
Authority
JP
Japan
Prior art keywords
heat
powder
molecular structure
coating
mica powder
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
Application number
JP21946691A
Other languages
Japanese (ja)
Other versions
JP2929332B2 (en
Inventor
Isao Watanabe
勲 渡辺
Minoru Tadokoro
実 田所
Kazumasa Okita
和正 沖田
Keizo Okubo
慶三 大久保
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.)
Okitsumo Inc
Hitachi Appliances Inc
Original Assignee
Okitsumo Inc
Hitachi Home Tech Ltd
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 Okitsumo Inc, Hitachi Home Tech Ltd filed Critical Okitsumo Inc
Priority to JP21946691A priority Critical patent/JP2929332B2/en
Publication of JPH0556855A publication Critical patent/JPH0556855A/en
Application granted granted Critical
Publication of JP2929332B2 publication Critical patent/JP2929332B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Abstract

PURPOSE:To obtain a cooker excellent in cleaning and clean properties by forming a coat film composed of polysiloxane containing specified heat-resistant crack-preventing agents on surface where dirt adheres through cooking. CONSTITUTION:As coating raw materials, 20-29wt.% of methyl polysiloxane having a three-dimensional reticulated molecular structure and 0.1-5wt.% of polysiloxane having a linear-chain molecular structure are used. As heat-resistant crack-preventing agents, flake substances or fibrous substances selected from mica powder, metal-oxide coated mica powder, graphite, talc, plate-like iron oxide pigment, flake metallic powder, and potassium titanate fiber are employed as essential components. Besides the above, coloring material, filler and additives are added, and the coating is applied on the surfaces of a top plate 3 and a drip plate 4 of a cooker or on the surface of a cooking compartment and heated to cure it. Thereby, the coating film itself does not change in color, and dirt that can not be wiped off is not formed.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明はガステーブル、オーブン
レンジ等調理物を加熱して調理する調理器具に関するも
ので、器具のトッププレートや調理室内が調理物から出
る汁や油等によって汚染されるのを防止するものであ
る。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a cooking utensil such as a gas table and a microwave oven which heats and cooks cooking food, and the top plate of the cooking utensil and the cooking chamber are contaminated by juice, oil and the like from the cooking food. To prevent this.

【0002】[0002]

【従来の技術】図1は従来のガステーブルを示し、この
ものは器体1内の中央にグリル部を配設し、上面をトッ
ププレート3で覆い、そのトッププレート3の左右にバ
ーナ4、汁受皿5、五徳6よりなるこんろ部7を配設
し、魚を焼く場合にはグリル部2を使用し、煮物その他
の調理はこんろ部7上で行なっていた。
2. Description of the Related Art FIG. 1 shows a conventional gas table, in which a grill portion is arranged in the center of a body 1, an upper surface is covered with a top plate 3, and burners 4 are provided on the left and right of the top plate 3. The cooking stove portion 7 composed of the soup saucer 5 and the Gotoku 6 was provided, and the grill portion 2 was used when fish was grilled, and the cooked food and other foods were cooked on the cooking stove portion 7.

【0003】[0003]

【発明が解決しようとする課題】上記従来のガステーブ
ルではトッププレート3や汁受皿5に耐熱性や汚染物の
ふき取りを考慮して例えばステンレス材や表面にホーロ
ー塗装したもの、あるいはフッ素樹脂加工したもの(例
えば実開昭64−41804号公報)が用いられている
が、ホーロー塗装したものは価格が高く、全体重量が大
幅に増加する欠点があり、また表面が硬度に出来ている
ため、金属物がぶつかると割れ等が発生する欠点があ
り、またフッ素樹脂加工のものは樹脂製のたわし等でふ
くとフッ素樹脂がはがれる欠点があり、最近ではステン
レス製のものが大半を占めるようになっている。
In the conventional gas table described above, the top plate 3 and the soup tray 5 are made of, for example, a stainless material, a enamel coating on the surface, or a fluororesin processing in consideration of heat resistance and wiping of contaminants. Although the one (for example, Japanese Utility Model Laid-Open No. 64-41804) is used, the enamel coated product is expensive and has a drawback that the total weight is significantly increased, and the surface is made hard so that the metal is used. There is a defect that cracks etc. will occur when objects hit, and the fluororesin processed one has the drawback that the fluororesin will peel off when wiped with a resin scrubber etc. Recently, stainless steel has become the majority. There is.

【0004】しかしこのものでもこんろ部7上に鍋等を
載せて調理を繰返すと、やがて調理物から出た汁や油
分、煤煙等がこびりつき、ふき取っても落ちない欠点が
あった。
However, even with this product, if a pot or the like is placed on the stove portion 7 and the cooking is repeated, the juice, oil, soot, etc. from the food will eventually stick to the product and will not fall off even if wiped off.

【0005】このことはオーブンレンジ等他の調理器具
でも同様であり食品から出た汁や油分等が調理庫内にこ
びりつき、ふき取っても落ちないものであり、早急にそ
の対策がせまられている。
This is also true of other cooking utensils such as a microwave oven, so that juice and oil from foods will stick to the inside of the cooking cabinet and will not fall off even if wiped off. Immediate countermeasures are required. ..

【0006】[0006]

【課題を解決するための手段】本発明は上記の欠点を解
決するためになされたもので、調理によって汚れが付着
する面に三次元網目状分子構造をもつメチルポリシロキ
サン及び直鎖状分子構造をもつポリシロキサンと、雲母
粉、金属酸化物被覆雲母粉、黒鉛、タルク、板状酸化鉄
顔料、鱗片状金属粉、チタン酸カリ繊維の内から選ばれ
る鱗片状物質或いは繊維状物質の単品もしくは混合物を
必須の主成分とする耐熱耐汚染性被膜被覆材を被覆し、
加熱硬化させたものである。
The present invention has been made to solve the above-mentioned drawbacks, and is a methylpolysiloxane having a three-dimensional network molecular structure and a linear molecular structure on the surface to which dirt is attached by cooking. With polysiloxane having mica powder, metal oxide-coated mica powder, graphite, talc, plate-shaped iron oxide pigment, scaly metal powder, potassium titanate fiber, or a scaly substance or a fibrous substance alone or Coated with a heat- and stain-resistant coating material whose mixture is an essential component
It was cured by heating.

【0007】本発明でいう三次元網目状分子構造をもつ
メチルポリシロキサンとは、通常、耐熱塗料に多く用い
られているメチルフェニルポリシロキサンと異なり、硅
素原子に直接結合する有機基としてフェニル基を含まず
メチル基だけを有するもので、末端に水酸基を残した構
造で保存し最終用途において脱水縮合による硬化をおこ
ない被膜を形成するものである。メチル基はフェニル基
と比べて分子量がはるかに小さいため、メチルポリシロ
キサンは加熱減量が少なく、加熱後の変色や熱による表
面劣化の少ない緻密な被膜を形成するものである。さら
に、好ましくは硅素原子1個に結合しているメチル基の
平均個数を0.5〜1.2と少なくすることによりさら
に加熱減量の少ない、架橋密度が高く熱硬化性の硬い被
膜を形成することが出来るが、耐熱亀裂性は良くない。
メチルフェニルポリシロキサンをメチルポリシロキサン
に混合することが出来るが、耐汚染性を低下させるた
め、全ポリシロキサン中の20wt%以下であることが
好ましい。
The methyl polysiloxane having a three-dimensional network molecular structure referred to in the present invention is different from methyl phenyl polysiloxane which is usually used in heat-resistant paint, and a phenyl group is used as an organic group directly bonded to a silicon atom. It does not contain a methyl group, and it is stored in a structure with a hydroxyl group remaining at the end and cured by dehydration condensation in the final application to form a film. Since the methyl group has a much smaller molecular weight than the phenyl group, the methylpolysiloxane has a small loss on heating and forms a dense film with little discoloration after heating and surface deterioration due to heat. Further, preferably, the average number of methyl groups bonded to one silicon atom is reduced to 0.5 to 1.2 to form a hard coating film having a small crosslinking loss and a high crosslinking density and a high thermosetting property. However, the heat crack resistance is not good.
Methylphenylpolysiloxane can be mixed with methylpolysiloxane, but it is preferably 20 wt% or less based on the total polysiloxane in order to reduce stain resistance.

【0008】直鎖状分子構造をもつポリシロキサンは、
表面張力が一般の有機油や溶剤に比べて非常に小さく、
また多くの物質に対して親和性、溶解性が小さいため離
型剤としての働きを持っている。化学的に不活性である
ため耐熱性に優れている上、生理的にも無毒といえる。
直鎖状分子構造をもつポリシロキサンの種類としては硅
素原子に直接結合する有機基としてメチル基だけを有す
るメチルポリシロキサン、メチル基とフェニル基の両方
をもつメチルフェニルポリシロキサン、メチル基と水素
原子をもつメチルハイドロジェンポリシロキサンが挙げ
られる。これは被覆物の耐汚染性を向上させる働きのも
のであるが、被覆材不揮発成分中、0.1〜5wt%の
範囲で含有することが望ましい。それ以上に含有させる
と被膜が熱軟化しやすく傷つきやすくなる。
Polysiloxane having a linear molecular structure is
The surface tension is very small compared to general organic oils and solvents,
In addition, since it has low affinity and solubility for many substances, it functions as a release agent. Since it is chemically inert, it has excellent heat resistance and is physiologically nontoxic.
Types of polysiloxane having a linear molecular structure include methyl polysiloxane having only a methyl group as an organic group directly bonded to a silicon atom, methylphenyl polysiloxane having both a methyl group and a phenyl group, a methyl group and a hydrogen atom. Methyl hydrogen polysiloxane having This has the function of improving the stain resistance of the coating, but it is desirable to contain it in the range of 0.1 to 5 wt% in the nonvolatile component of the coating material. If it is contained in a larger amount, the coating tends to be softened by heat and is easily scratched.

【0009】雲母粉、金属酸化物被覆雲母粉、黒鉛、タ
ルク、板状酸化鉄顔料、鱗片状金属粉、チタン酸カリ繊
維の内から選ばれる粒子径1〜100μm、厚さ0.0
1〜10μmの鱗片状物質、或いは繊維径0.1〜5μ
m、繊維長10〜1000μmの繊維状物質の単品もし
くは混合物は、塗膜のひび割れを防止し、耐熱亀裂性を
向上させる働きがあり、被覆材不揮発成分の5〜80w
t%の範囲で使用することが好ましい。
Mica powder, metal oxide-coated mica powder, graphite, talc, plate-shaped iron oxide pigment, scaly metal powder, potassium titanate fiber, having a particle size of 1 to 100 μm and a thickness of 0.0.
1 to 10 μm scale-like substance or fiber diameter 0.1 to 5 μm
m or a fibrous substance having a fiber length of 10 to 1000 μm has a function of preventing cracks in the coating film and improving heat crack resistance, and is 5 to 80 w of the non-volatile component of the coating material.
It is preferably used in the range of t%.

【0010】また美観を目的とする彩色のための着色材
や、増量材を被覆材不揮発成分中に0〜75wt%混合
することができる。さらに、添加剤として硬化剤や沈降
防止剤を0〜5wt%混合することにより被覆材の加熱
硬化を低温短時間で行なうことや、被覆材のレオロジー
的な調整を行なうことができる。
Further, a coloring material for coloring for the purpose of aesthetics and an extender can be mixed in the non-volatile component of the coating material in an amount of 0 to 75% by weight. Furthermore, by mixing 0 to 5 wt% of a curing agent or an anti-settling agent as an additive, the coating material can be heat-cured at a low temperature for a short time, and the coating material can be rheologically adjusted.

【0011】これら不揮発成分と、揮発成分としてアル
コール、ケトン、芳香族炭化水素、その他の有機溶剤の
単品或いは混合溶剤を希釈剤として含む耐熱耐汚染性被
膜被覆材をガステーブルのトッププレートや汁受皿、オ
ーブンレンジの調理庫内に被覆し、好ましくは250℃
〜450℃の温度で加熱硬化することにより、それ自体
が熱によって変色したり、調理物から出る汁や油、煤煙
などによってふき取れない汚染となる現象もない清掃
性、密着性に優れた調理器具を提供することが出来る。
A gas-table top plate or a soup saucer is provided with a heat-resistant and stain-resistant coating material containing these non-volatile components and alcohols, ketones, aromatic hydrocarbons or other organic solvents as volatile components as a diluent or a mixed solvent as a diluent. , Coated in the microwave oven cooker, preferably 250 ℃
By heating and hardening at a temperature of ~ 450 ° C, the food itself discolors due to heat, and there is no phenomenon that it becomes a stain that cannot be wiped off by the juice, oil, soot, etc. from the food being cooked. Equipment can be provided.

【0012】また、本発明の耐熱耐汚染性被膜被覆材の
被覆厚には特に制限はないが一般に5〜100μmの被
覆厚が好ましい。これ以下の被覆厚では均一に被覆する
ことが難かしく、またこれ以上の被覆厚では経済的でな
い上、加熱時にひび割れが生じやすくなる。なお、耐熱
耐汚染性被膜被覆材の被覆に関してその方法や加熱硬化
の方法は従来公知のいずれの方法でもよい。
The coating thickness of the heat and stain resistant coating coating material of the present invention is not particularly limited, but a coating thickness of 5 to 100 μm is generally preferable. If the coating thickness is less than this, it is difficult to coat uniformly, and if the coating thickness is more than this, it is not economical and cracks are likely to occur during heating. Regarding the coating of the heat- and stain-resistant stain-resistant coating material, any known method may be used as the method or the method of heat curing.

【0013】[0013]

【実施例】次に本発明を実施例に基づき、さらに詳細に
説明する。図1は本発明に係るガステーブルであり、そ
の構造、作用は上記従来の技術で述べた通りであり、説
明を省略する。また図2は一般的なオーブンレンジを示
し、8は器体、9は調理庫で、調理物はこの調理庫9内
で加熱調理される。
EXAMPLES The present invention will be described in more detail based on examples. FIG. 1 shows a gas table according to the present invention, the structure and operation of which are the same as those described in the conventional art, and the description thereof will be omitted. Further, FIG. 2 shows a general microwave oven, 8 is a body, 9 is a cooking cabinet, and cooked food is cooked in the cooking cabinet 9.

【0014】本発明において、上記耐熱耐汚染性被膜被
覆材は図1のトッププレート3、汁受皿5、図2の調理
庫9の表面に被覆される。
In the present invention, the heat- and stain-resistant coating film coating material is coated on the surfaces of the top plate 3, the juice tray 5 of FIG. 1 and the cooking cabinet 9 of FIG.

【0015】以下その被覆材について表を参照しながら
説明する。
The coating material will be described below with reference to the table.

【0016】表1は被覆材減量樹脂の耐熱性能に関する
総合評価結果である。
Table 1 shows the comprehensive evaluation results regarding the heat resistance performance of the coating material reducing resin.

【0017】[0017]

【表1】 [Table 1]

【0018】ここで樹脂(1)はメチルフェニルポリシ
ロキサン例えば商品名KR−311信越化学社製、樹脂
(2)はメチルフェニルポリシロキサン例えば商品名K
R−282信越化学社製、樹脂(3)はメチルポリシロ
キサン例えば商品名KR−240信越化学社製、樹脂
(4)はアルキッド変性シリコーン樹脂例えば商品名K
R−206信越化学社製、樹脂(5)はエポキシ変性シ
リコーン樹脂例えば商品名ES1001信越化学社製、
樹脂(6)は四ふっ化エチレン樹脂、樹脂(7)は四ふ
っ化エチレン樹脂とポリエーテルサルホン樹脂の共重
合、樹脂(8)はビスフェノール型エポキシ樹脂であ
る。このとき、樹脂50部に雲母粉10部、着色材とし
て酸化チタン38部、沈降防止剤2部混合し、これに希
釈剤を用いて粘度を岩田カップで15秒に調整し、一般
的なエアスプレーガンを用い被覆厚を30μmとした。
またこの評価に用いた基材は標準的なステンレス板(S
US−304)を用いた。加熱硬化の条件としては電気
オーブンを用い80℃で予備乾燥したあと400℃で2
0分の加熱を行なった。
Here, the resin (1) is methylphenyl polysiloxane, for example, trade name KR-311 manufactured by Shin-Etsu Chemical Co., Ltd., and the resin (2) is methylphenyl polysiloxane, for example trade name K.
R-282 manufactured by Shin-Etsu Chemical Co., Ltd., resin (3) is methyl polysiloxane, for example, trade name KR-240 Shin-Etsu Chemical Co., Ltd., resin (4) is alkyd-modified silicone resin, for example trade name K.
R-206 manufactured by Shin-Etsu Chemical Co., Ltd., resin (5) is an epoxy-modified silicone resin, for example, ES1001 manufactured by Shin-Etsu Chemical Co., Ltd.,
The resin (6) is an ethylene tetrafluoride resin, the resin (7) is a copolymer of an ethylene tetrafluoride resin and a polyether sulfone resin, and the resin (8) is a bisphenol type epoxy resin. At this time, 50 parts of resin were mixed with 10 parts of mica powder, 38 parts of titanium oxide as a coloring material, and 2 parts of an anti-settling agent. The coating thickness was 30 μm using a spray gun.
The base material used for this evaluation is a standard stainless steel plate (S
US-304) was used. The conditions for heat curing are an electric oven, predrying at 80 ° C, and then 2 at 400 ° C.
Heating for 0 minutes was performed.

【0019】表2は三次元網目状分子構造を持つメチル
ポリシロキサンの耐熱亀裂防止材に関する評価結果であ
る。
Table 2 shows the evaluation results of the heat-resistant crack preventing material of methylpolysiloxane having a three-dimensional network molecular structure.

【0020】[0020]

【表2】 [Table 2]

【0021】ここで耐熱亀裂防止材(1)はSiC微粉
例えばGMF−12H太平洋ランダム社製、耐熱亀裂防
止材(2)は鱗片黒鉛例えば4A東亜黒鉛精錬社製、耐
熱亀裂防止材(3)は板状酸化鉄顔料例えばMIO−2
F日本無機化学工業社製、耐熱亀裂防止材(4)は硅石
粉例えばシルシックT−3大東産業社製、耐熱亀裂防止
材(5)は金属酸化物被覆雲母粉例えばIriodin
100メルク社製、耐熱亀裂防止材(6)はタルク例え
ばタルクMS日本タルク社製、耐熱亀裂防止材(7)は
雲母粉例えばA−1山口雲母工業社製、耐熱亀裂防止材
(8)は鱗片状アルミニウム粉例えば1100NA東洋
アルミ社製、耐熱亀裂防止材(9)はチタン酸カリ繊維
例えばBタイプ久保田鉄工社製、耐熱亀裂防止材(1
0)は酸化鉄例えば弁柄No.112森下弁柄社製、耐
熱亀裂防止材(11)はホワイトカーボン例えばサイロ
イド978富士デビィソン社製である。このとき、被覆
原料樹脂(3)を60部、着色材として酸化チタン18
部、沈降防止剤2部、耐熱亀裂防止材20部混合し、こ
れをトルエンとブタノールを1:1で混合した希釈剤で
粘度を岩田カップで15秒に調整した。その他の条件は
被覆原料樹脂の評価と同一である。
Here, the heat-resistant crack prevention material (1) is SiC fine powder such as GMF-12H Taiheiyo Random Co., Ltd., the heat-resistant crack prevention material (2) is scaly graphite such as 4A Toa Graphite Smelting Co., and the heat-resistant crack prevention material (3) is Plate-shaped iron oxide pigments such as MIO-2
F Japan Inorganic Chemical Industry Co., Ltd., heat resistant crack prevention material (4) is silica powder such as Silchic T-3 Daito Sangyo Co., heat resistant crack prevention material (5) is metal oxide coated mica powder such as Iriodin
100 Merck, heat-resistant crack prevention material (6) is talc, for example, talc MS Nippon Talc Co., heat-resistant crack prevention material (7) is mica powder, for example, A-1 Yamaguchi Mica Industry Co., Ltd., heat-resistant crack prevention material (8) is Scale-like aluminum powder such as 1100NA manufactured by Toyo Aluminum Co., Ltd., a heat-resistant crack preventive material (9) is potassium titanate fiber such as B type manufactured by Kubota Iron Works Co., Ltd., a heat-resistant crack preventive material (1).
0) is iron oxide such as Rouge No. The heat-resistant crack prevention material (11) manufactured by Morishita Benji Co., Ltd. is white carbon, for example, Cyloid 978 manufactured by Fuji Devison. At this time, 60 parts of the coating raw material resin (3), titanium oxide 18 as a coloring material
Parts, 2 parts of anti-settling agent, and 20 parts of heat-resistant crack preventing material were mixed, and the viscosity was adjusted to 15 seconds with an Iwata cup with a diluent in which toluene and butanol were mixed at a ratio of 1: 1. Other conditions are the same as the evaluation of the coating material resin.

【0022】表3は被覆物の耐汚染性に関する評価結果
である。
Table 3 shows the evaluation results regarding the stain resistance of the coating.

【0023】[0023]

【表3】 [Table 3]

【0024】配合例に示される不揮発成分からなる被覆
材を図1のトッププレート3、汁受皿4あるいは図2の
調理庫9の表面に被覆し、加熱硬化させた後、200時
間程調理を行ない、その変色状態を調べた。
The surface of the top plate 3, the soup saucer 4 of FIG. 1 or the cooking cabinet 9 of FIG. 2 is coated with the coating material made of the non-volatile components shown in the formulation example, and after heating and curing, cooking is performed for about 200 hours. , And examined the discolored state.

【0025】表4は被覆材の加熱硬化条件について検討
した結果である。
Table 4 shows the results of examining the heat curing conditions of the coating material.

【0026】[0026]

【表4】 [Table 4]

【0027】被覆材としては配合(4)を用いた。これ
にトルエンとブタノールを1:1で混合した希釈剤を用
いて粘度を岩田カップで15秒に調整し、一般的なエア
スプレーガンを用い被覆厚を30μmに塗装した。また
この評価に用いた基材は標準的なステンレス板(SUS
−304)を用いた。加熱硬化の条件としては電気オー
ブンを用い80℃で予備乾燥した後、所定の温度で加熱
硬化した。
Formula (4) was used as the coating material. The viscosity was adjusted to 15 seconds with an Iwata cup using a diluent in which toluene and butanol were mixed at a ratio of 1: 1 and the coating thickness was applied to 30 μm using a general air spray gun. The base material used for this evaluation is a standard stainless steel plate (SUS
-304) was used. As conditions for heat curing, an electric oven was used for preliminary drying at 80 ° C. and then heat curing at a predetermined temperature.

【0028】なお表中二重丸は特性が極めて良好、○は
特性が良好、△は実用可能、×は実用的でないことを示
す。
In the table, double circles indicate extremely good characteristics, ◯ indicates good characteristics, Δ indicates practicable, and x indicates impractical.

【0029】以上の評価ををした結果、被覆材原料樹脂
としては耐熱後の密着性、変色に優れる樹脂(1)、
(2)、(3)が選ばれるが、最も良好なものは光沢劣
化の少ない樹脂(3)であった。また樹脂(3)の耐熱
亀裂防止材として効果のあったものは、鱗片状物質であ
る耐熱亀裂防止材(2)、耐熱亀裂防止材(3)、耐熱
亀裂防止材(5)、耐熱亀裂防止材(6)、耐熱亀裂防
止材(7)、耐熱亀裂防止材(8)と、繊維状物質であ
る耐熱亀裂防止材(9)であった。さらに被覆物の耐汚
染性に関する評価では、配合(4)で最も良好な結果、
また配合(2)と配合(5)で良好な結果が得られた。
加熱硬化条件としては、150℃20分から550℃2
0分まで実用可能であるが、耐汚染性を考慮した場合、
250℃20分から450℃20分の範囲が最も良好で
あった。
As a result of the above evaluation, as the coating material raw material resin, the resin (1) which is excellent in adhesion and discoloration after heat resistance,
Although (2) and (3) were selected, the most preferable one was the resin (3) with less gloss deterioration. Further, what has been effective as a heat-resistant crack preventive material for the resin (3) is a heat-resistant crack preventive material (2), a heat-resistant crack preventive material (3), a heat-resistant crack preventive material (5), a heat-resistant crack preventive which is a scale-like substance. The material (6), the heat-resistant crack preventing material (7), the heat-resistant crack preventing material (8), and the heat-resistant crack preventing material (9) which is a fibrous substance. Furthermore, in the evaluation of the stain resistance of the coating, the best result was obtained with the compound (4),
Also, good results were obtained with the formulations (2) and (5).
The heat curing condition is 150 ° C. for 20 minutes to 550 ° C. 2
It can be used for up to 0 minutes, but when considering stain resistance,
The best range was from 20 minutes at 250 ° C to 20 minutes at 450 ° C.

【0030】[0030]

【発明の効果】以上のように本発明は三次元網目状分子
構造をもつメチルポリシロキサン及び直鎖状分子構造を
もつポリシロキサンと、雲母粉、金属酸化物被覆雲母
粉、黒鉛、タルク、板状酸化鉄顔料、鱗片状金属粉、チ
タン酸カリ繊維の内から選ばれる鱗片状物質或いは繊維
状物質の単品もしくは混合物を必須の主成分とする耐熱
耐汚染性被膜被覆材を調理器具の調理物から出る汁や油
等によって汚染される面に被覆し、加熱硬化させること
によって、それ自体が熱によって変色することも、ふき
取れない汚染となる現象もない、清掃性、密着性に優れ
た調理器具を提供することが出来るものである。
As described above, according to the present invention, methylpolysiloxane having a three-dimensional network molecular structure and polysiloxane having a linear molecular structure, mica powder, metal oxide-coated mica powder, graphite, talc, and plate are used. Cooked cookware with a heat- and stain-resistant coating material containing a scale-like substance or a mixture of scale-like substances or fibrous substances selected from powdery iron oxide pigments, scale-like metal powder and potassium titanate fiber as an essential main component By coating the surface that is contaminated with juice or oil that comes out of it, and heating and curing it, there is no discoloration due to heat, and there is no phenomenon of contamination that cannot be wiped off. An instrument can be provided.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明に係るガステーブルの一部分解斜視図で
ある。
FIG. 1 is a partially exploded perspective view of a gas table according to the present invention.

【図2】本発明に係るオーブンレンジの斜視図である。FIG. 2 is a perspective view of a microwave oven according to the present invention.

【符号の説明】[Explanation of symbols]

3 トッププレート 5 汁受皿 9 調理庫 3 Top plate 5 Soup saucer 9 Cookery

───────────────────────────────────────────────────── フロントページの続き (72)発明者 沖田 和正 三重県名張市蔵持町芝出1109番地7 オキ ツモ株式会社内 (72)発明者 大久保 慶三 三重県名張市蔵持町芝出1109番地7 オキ ツモ株式会社内 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Kazumasa Okita 1109, Shibaide, Shimochi-machi, Nabari-shi, Mie Prefecture, Okitsumo Co., Ltd. Within the corporation

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 ガステーブル、オーブンレンジ等調理物
を加熱して調理する調理器具において、前記調理によっ
て汚れが付着する面に三次元網目状分子構造をもつメチ
ルポリシロキサン及び直鎖状分子構造をもつポリシロキ
サンと、雲母粉、金属酸化物被覆雲母粉、黒鉛、タル
ク、板状酸化鉄顔料、鱗片状金属粉、チタン酸カリ繊維
の内から選ばれる鱗片状粉末或いは繊維状粉末の単品も
しくは混合物を必須の主成分とする耐熱耐汚染性被膜被
覆材を被覆し、加熱硬化させたことを特徴とする調理器
具。
1. A cookware for heating a cooked food, such as a gas table or a microwave oven, to prepare methylpolysiloxane having a three-dimensional network molecular structure and a linear molecular structure on the surface to which dirt is attached by the cooking. And a mixture of polysiloxane and mica powder, metal oxide-coated mica powder, graphite, talc, plate-shaped iron oxide pigment, scale-like metal powder, potassium titanate fiber, or a scale-like powder or fibrous powder. A cooking utensil characterized by being coated with a heat- and stain-resistant coating film coating containing, as an essential component, and cured by heating.
【請求項2】 請求項1記載のものにおいて、耐熱耐汚
染性被膜被覆材は三次元網目状分子構造をもつメチルポ
リシロキサンが0.1〜5wt%、雲母粉、金属酸化物
被覆雲母粉、黒鉛、タルク、板状酸化鉄顔料、鱗片状金
属粉、チタン酸カリ繊維の内から選ばれる粒子径1〜1
00μm、厚さ0.01〜10μmの鱗片状物質、或い
は繊維径0.1〜5μm、繊維長10〜1000μmの
繊維状物質の単品もしくは混合物が5〜80wt%、着
色材、増量材が0〜75wt%、添加剤が0〜5wt%
である不揮発成分からなることを特徴とする調理器具。
2. The heat- and stain-resistant coating material according to claim 1, wherein the methylpolysiloxane having a three-dimensional network molecular structure is 0.1 to 5 wt%, mica powder, metal oxide-coated mica powder, Particle size 1 to 1 selected from graphite, talc, plate-shaped iron oxide pigment, scale-like metal powder, potassium titanate fiber
5 to 80 wt% of a scaly substance having a thickness of 0.01 μm and a thickness of 0.01 to 10 μm, or a fibrous substance having a fiber diameter of 0.1 to 5 μm and a fiber length of 10 to 1000 μm, 5 to 80 wt%, and a coloring material and an extender to 0. 75 wt%, 0 to 5 wt% additive
A cooking utensil characterized by comprising a non-volatile component.
JP21946691A 1991-08-30 1991-08-30 kitchenware Expired - Fee Related JP2929332B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP21946691A JP2929332B2 (en) 1991-08-30 1991-08-30 kitchenware

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP21946691A JP2929332B2 (en) 1991-08-30 1991-08-30 kitchenware

Publications (2)

Publication Number Publication Date
JPH0556855A true JPH0556855A (en) 1993-03-09
JP2929332B2 JP2929332B2 (en) 1999-08-03

Family

ID=16735878

Family Applications (1)

Application Number Title Priority Date Filing Date
JP21946691A Expired - Fee Related JP2929332B2 (en) 1991-08-30 1991-08-30 kitchenware

Country Status (1)

Country Link
JP (1) JP2929332B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010525095A (en) * 2007-04-18 2010-07-22 セブ エス.アー. Anti-adhesion coating with improved hydrophobicity
JP4791674B2 (en) * 2000-05-18 2011-10-12 関西ペイント株式会社 Multi-layer coating formation method
CN109679397A (en) * 2017-08-16 2019-04-26 宜宾天原集团股份有限公司 Silicone resin solvent and its application

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4791674B2 (en) * 2000-05-18 2011-10-12 関西ペイント株式会社 Multi-layer coating formation method
JP2010525095A (en) * 2007-04-18 2010-07-22 セブ エス.アー. Anti-adhesion coating with improved hydrophobicity
CN109679397A (en) * 2017-08-16 2019-04-26 宜宾天原集团股份有限公司 Silicone resin solvent and its application

Also Published As

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