JPH06147502A - Cooker, contaminant preventing cover material and painting method thereof - Google Patents
Cooker, contaminant preventing cover material and painting method thereofInfo
- Publication number
- JPH06147502A JPH06147502A JP29697892A JP29697892A JPH06147502A JP H06147502 A JPH06147502 A JP H06147502A JP 29697892 A JP29697892 A JP 29697892A JP 29697892 A JP29697892 A JP 29697892A JP H06147502 A JPH06147502 A JP H06147502A
- Authority
- JP
- Japan
- Prior art keywords
- polysiloxane
- silicate
- mixture
- parts
- cooking
- 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.)
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- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
【産業上の利用分野】本発明はガステーブル等を用い加
熱調理したときに吹きこぼれたり、飛散した食品の汁や
油が付着し、固化して出来た汚染物の除去を容易にし、
器具のトッププレート、汁受皿やグリルの庫内等の汚染
防止を図った調理器具とその汚染防止被覆材及びその塗
装方法に関するものである。BACKGROUND OF THE INVENTION The present invention makes it easy to remove contaminants that are solidified by spilling or spattering food juice or oil when heated and cooked using a gas table, etc.
The present invention relates to a cooking utensil for preventing contamination of the top plate of the utensil, the soup saucer and the inside of the grill, a coating material for preventing the contamination, and a coating method thereof.
【従来の技術】図1は一般的な調理器具の一例であるガ
ステーブルの斜視図を示し、従来は器体1内の中央にグ
リル部2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 is a perspective view of a gas table which is an example of a general cooking utensil. Conventionally, a grill portion 2 is arranged in the center of a body 1 and an upper surface is covered with a top plate 3. On the left and right of the top plate 3 are arranged a burner section 7, a soup saucer 5, and a stove section 7 consisting of Gotoku 6. When grilling fish, the grill section 2 is used. I was doing in.
【発明が解決しようとする課題】上記従来の調理器具の
一例であるガステーブルではトッププレート3や汁受皿
5に耐熱性や固着した汚染物の除去を考慮して例えばス
テンレス材や金属材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64−41
804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こするとフッ素樹脂がはが
れたり、耐熱性に欠けるため次第に熱劣化して対汚染性
が低下し、繰返し使用すると汚染物が除去し難くなる等
の欠点がある。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。しかし、このものでも汚染物が
除去し難く、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くなるという欠点があった。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。In the gas table, which is an example of the conventional cooking utensil described above, heat resistance and removal of contaminants adhered to the top plate 3 and the soup saucer 5 are taken into consideration, for example, on the surface of stainless steel or metal. Enameled paint or fluororesin-processed (for example, actual development 64-41
No. 804 gazette) is used, but the enamel coating is expensive and has the drawback of increasing the overall weight significantly, and because the surface is made hard, cracks etc. occur when metal objects collide. In addition, the fluororesin-processed ones will peel off the fluororesin if it is rubbed with a resin scrubber, or the heat resistance will be lacking and the heat resistance will gradually deteriorate to reduce the contamination resistance. There are drawbacks such as difficulty in doing so. Recently, stainless steel has become the majority. However, even with this product, it is difficult to remove contaminants, and if you put a pot on the cooking stove 7 and repeat cooking, the juice, oil, soot, etc. from the food will stick to the cooking stove and will not fall off even if wiped off. was there. This is the same with other cooking utensils such as a microwave oven, so that juices and oils from foods stick to the inside of the cooking cabinet and do not fall off even if wiped off. Immediate countermeasures are required.
【課題を解決するための手段】本発明は上記の課題を解
決するためになされたもので、金属との密着性に優れる
変性ポリシロキサン及び鱗片状構造を持つ珪酸マグネシ
ウム、珪酸アルミニウムの珪酸塩化合物、鱗片状金属酸
化鉄顔料、黒鉛の単品もしくはこれらの混合物を主成分
とする被覆材を下塗り層とし、三次元網目状構造を形成
するメチル基またはメチル基及びフェニル基を含有した
ポリシロキサンと直鎖状の反応性ポリシロキサン及び鱗
片状構造を持つ珪酸マグネシウム、珪酸アルミニウムの
珪酸塩化合物、鱗片状金属酸化鉄顔料、黒鉛の単品もし
くはこれらの混合物を主成分とする被覆材を上塗り層と
して加熱硬化させた二重構造からなる耐熱耐汚染性被膜
被覆を調理によって汚れが付着する調理器具のグリル
部、トッププレート、汁受皿、調理庫等に施したもので
ある。二重構造からなる耐熱耐汚染性被膜被覆材は、下
塗り層を変性ポリシロキサン及び鱗片状構造を持つ珪酸
マグネシウム、珪酸アルミニウムの珪酸塩化合物、鱗片
状金属酸化鉄顔料、黒鉛の中から選ばれる厚さ10μm
以下でアスペクト比0.1〜15の鱗片状物質の単品も
しくはこれらの混合物5〜50重量部を主成分とし、着
色材、増量材が0〜40重量部の割合で含む混合物でな
るものとし、また、上塗り層は三次元網目状構造を形成
するメチル基70〜100MOL%、フェニル基0〜3
0MOL%からなるポリシロキサンの単品もしくはこれ
らの混合物で50〜99重量部及び直鎖状の反応性ポリ
シロキサン1〜20重量部と、鱗片状構造を持つ珪酸マ
グネシウム、珪酸アルミニウムの珪酸塩化合物、鱗片状
金属酸化鉄顔料、黒鉛の中から選ばれる厚さ10μm以
下でアスペクト比0.1〜15の鱗片状物質の単品もし
くはこれらの混合物5〜30重量部を主成分とし、着色
材、増量材が0〜60重量部の割合で含む混合物でなる
ものとした。二重構造からなる耐熱耐汚染性被膜被覆材
の被覆は、下塗り層が乾燥膜厚で3〜70μm、上塗り
層は乾燥膜厚で5〜80μmに仕上がるように塗装し、
200〜450℃の温度で10〜30分間の加熱乾燥し
て被覆化した。The present invention has been made to solve the above problems, and is a modified polysiloxane having excellent adhesion to metal and magnesium silicate having a scaly structure, or a silicate compound of aluminum silicate. , A scaly metal iron oxide pigment, a single material of graphite or a coating material containing a mixture thereof as a main component is used as an undercoat layer, and is directly combined with a polysiloxane containing a methyl group or a methyl group and a phenyl group to form a three-dimensional network structure. Heat-cured with a coating material consisting mainly of chain-like reactive polysiloxane and scale-like magnesium silicate, aluminum silicate silicate compound, scale-like iron oxide oxide pigment, single graphite or a mixture thereof as an overcoat layer The grill and top plate of cookware to which dirt is attached by cooking with a heat-resistant and stain-resistant coating with a double structure Juice saucer, it is that has been subjected to the cooking chamber and the like. Heat- and stain-resistant coating coating material consisting of double structure is a thickness selected from modified polysiloxane for undercoat layer and magnesium silicate having scale-like structure, silicate compound of aluminum silicate, scale-like iron oxide oxide pigment, and graphite. 10 μm
Below, it shall be a mixture containing 5 to 50 parts by weight of a scaly substance having an aspect ratio of 0.1 to 15 or a mixture thereof as a main component, and a coloring material and an extender in a ratio of 0 to 40 parts by weight, The overcoat layer is a methyl group 70 to 100 MOL% and a phenyl group 0 to 3 forming a three-dimensional network structure.
50 to 99 parts by weight of a polysiloxane consisting of 0 MOL% or a mixture thereof, and 1 to 20 parts by weight of a linear reactive polysiloxane, magnesium silicate having a scaly structure, a silicate compound of aluminum silicate, and a scale. Metallic iron oxide pigments, graphite having a thickness of 10 μm or less and an aspect ratio of 0.1 to 15 and a scale-like substance alone or 5 to 30 parts by weight of a mixture thereof as a main component. A mixture containing 0 to 60 parts by weight was used. The heat- and stain-resistant coating material having a double structure is coated so that the undercoat layer has a dry film thickness of 3 to 70 μm and the overcoat layer has a dry film thickness of 5 to 80 μm.
Coating was performed by heating and drying at a temperature of 200 to 450 ° C. for 10 to 30 minutes.
【作用】変性ポリシロキサン及び鱗片状構造を持つ珪酸
マグネシウム、珪酸アルミニウムの珪酸塩化合物、鱗片
状金属酸化鉄顔料、黒鉛の単品もしくはこれらの混合物
を主成分とする下塗り層と、三次元網目状構造を形成す
るメチル基またはメチル基及びフェニル基を含有したポ
リシロキサンと直鎖状の反応性ポリシロキサン及び鱗片
状構造を持つ珪酸マグネシウム、珪酸アルミニウムの珪
酸塩化合物、鱗片状金属酸化鉄顔料、黒鉛の単品もしく
はこれらの混合物を主成分とする被覆材を上塗り層とし
て加熱硬化させた二重構造からなる耐熱耐汚染性被膜被
覆は、被覆を施した器具のトッププレート、汁受皿やグ
リルの庫内等の、ひび割れ防止や柔軟性を向上させ、調
理物から出た汁や油のこびり付きをなくし、その作用の
永続性を持たせる。[Function] Silica having modified polysiloxane and scaly structure
Magnesium, silicate compounds of aluminum silicate, scales
Iron oxide pigments, graphite single products or their mixtures
To form a three-dimensional network structure with a subbing layer mainly composed of
A methyl group or a group containing a methyl group and a phenyl group.
Resiloxane with linear reactive polysiloxane and scale
Silicate of Magnesium Silicate and Aluminum Silicate with a Structure
Acid salt compound, scale-like metallic iron oxide pigment, graphite alone
Is a coating material containing these mixtures as the main component
Heat- and stain-resistant coating with double structure
The cover is the top plate of the coated appliance, the saucer or
Prevents cracks and improves flexibility in the inside of the rill
It eliminates the sticking of juice and oil that comes out of
Make it permanent.
【実施例】次に本発明を実施例に基づき詳細に説明す
る。図1は本発明の一実施例を施したガステーブルの斜
視図であり、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
ブンレンジの斜視図であり、図において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。
本発明において、図1のグリル部2、トッププレート
3、汁受皿5、図2の調理庫9等の調理によって汚れが
付着する面に、変性ポリシロキサン及び鱗片状構造を持
つ珪酸マグネシウム、珪酸アルミニウムの珪酸塩化合
物、鱗片状金属酸化鉄顔料、黒鉛の単品もしくはこれら
の混合物を主成分とする被覆材を下塗り層とし、三次元
網目状構造を形成するメチル基またはメチル基及びフェ
ニル基を含有したポリシロキサンと直鎖状の反応性ポリ
シロキサン及び鱗片状構造を持つ珪酸マグネシウム、珪
酸アルミニウムの珪酸塩化合物、鱗片状金属酸化鉄顔
料、黒鉛の単品もしくはこれらの混合物を主成分とする
被覆材を上塗り層として加熱硬化させた二重構造からな
る耐熱耐汚染性被膜被覆を施して構成した。以下上記耐
熱耐汚染性被膜被覆材について表を参照しながら説明す
る。表1は変性ポリシロキサンを下塗りに使用する理由
を示す。EXAMPLES Next, the present invention will be described in detail based on examples. FIG. 1 is a perspective view of a gas table to which an embodiment of the present invention is applied, and its structure and operation are as described in the above-mentioned conventional technique, and the description thereof will be omitted. FIG. 2 is a perspective view of a general microwave oven. In the figure, 8 is a body, 9 is a cooking cabinet, and food is cooked in the cooking cabinet 9.
In the present invention, the modified polysiloxane and magnesium silicate and aluminum silicate having a scale-like structure are attached to the surface of the grill portion 2, the top plate 3, the juice receiving tray 5 of FIG. Of the silicate compound, the scale-like metallic iron oxide pigment, the single material of graphite or a mixture thereof as a main component is used as an undercoat layer and contains a methyl group or a methyl group and a phenyl group forming a three-dimensional network structure. Top coat with polysiloxane and linear reactive polysiloxane and scale-like magnesium silicate, aluminum silicate silicate compound, scale-like iron oxide iron pigment, graphite single substance or a mixture containing these as main components. It was constructed by applying a heat-resistant and stain-resistant film coating having a double structure which was heat-cured as a layer. The heat resistant and stain resistant coating material will be described below with reference to the table. Table 1 shows the reasons for using the modified polysiloxane in the basecoat.
【表1】 下塗り層評価に用いた、下塗Aのメチルポリシロキサン
は例えば信越化学工業社製KR−220、下塗Bのメチ
ルフェニルポリシロキサンは例えば信越化学工業社製メ
チル基60MOL%とフェニル基40MOL%からなる
ポリシロキサンKR−282、下塗Cのアルキッド変性
ポリシロキサンは例えば東芝シリコーン社製TSR−1
80、下塗Dのポリエステル変性ポリシロキサンは東芝
シリコーン社製TSR−187、下塗Eのアクリル変性
ポリシロキサンは例えば東芝シリコーン社製TSR−1
70、下塗Fのエポキシ変性ポリシロキサンは東芝シリ
コーン社製TSR−194、それぞれの単品に、珪酸マ
グネシウム例えば堀クレー社製とカーボンブラック例え
ば三菱化成社製を混合分散した混合物を、下塗G〜下塗
Kはエポキシ変性ポリシロキサンと珪酸マグネシウムの
混合比を変化させ、カーボンブラックと混合分散した混
合物を、被膜で15〜20μmに被覆し、300℃の温
度15分間で加熱硬化を行なった。表2は変性ポリシロ
キサンに寄与する鱗片顔料の効果を示す。[Table 1] The methyl polysiloxane of the undercoat A used in the evaluation of the undercoat layer is, for example, KR-220 manufactured by Shin-Etsu Chemical Co., Ltd., and the methylphenylpolysiloxane of the undercoat B is, for example, a polycomprising 60 MOL% of methyl groups and 40 MOL% of phenyl groups manufactured by Shin-Etsu Chemical. The siloxane KR-282 and the alkyd-modified polysiloxane of the undercoat C are, for example, TSR-1 manufactured by Toshiba Silicone Co., Ltd.
80, the polyester-modified polysiloxane of the undercoat D is TSR-187 manufactured by Toshiba Silicone, and the acrylic-modified polysiloxane of the undercoat E is, for example, TSR-1 manufactured by Toshiba Silicone.
70, TSR-194 manufactured by Toshiba Silicone Co., Ltd. is an epoxy-modified polysiloxane of the undercoat F, and a mixture of magnesium silicate such as Hori Clay Co. and carbon black such as Mitsubishi Kasei Co., Ltd. is mixed and dispersed. Was mixed with carbon black by changing the mixing ratio of the epoxy-modified polysiloxane and magnesium silicate, and the mixture was coated to a thickness of 15 to 20 μm, followed by heat curing at a temperature of 300 ° C. for 15 minutes. Table 2 shows the effect of the scaly pigment on the modified polysiloxane.
【表2】 鱗片顔料の効果の確認に用いた珪酸マグネシウムは例え
ば堀クレー社製、珪酸アルミニウムは例えば堀クレー社
製、珪石粉例えば電気化学工業社製、硫酸バリウムは例
えば堺化学工業社製、炭酸カルシウムは例えば堀クレー
社製、鱗片状金属酸化物は例えば日本無機化学工業社
製、黒鉛は日本黒鉛社製の単品それぞれに、エポキシ変
性ポリシロキサンとカーボンブラックを混合分散した混
合物を、被膜で15〜20μmに被覆し、300℃の温
度15分間で加熱硬化を行なった。表3は三次元網目状
構造を形成するメチルポリシロキサンを上塗りに使用す
る理由を示す。[Table 2] Magnesium silicate used for confirming the effect of the scale pigment is, for example, Hori Clay Co., aluminum silicate is, for example, Hori Clay Co., silica powder, for example, Denki Kagaku Kogyo, barium sulfate is Sakai Chemical Co., Ltd., calcium carbonate is Hori Clay Co., scale-like metal oxides are manufactured by Nippon Inorganic Chemical Industry Co., Ltd., and graphite is manufactured by Nippon Graphite Co., Ltd. A mixture of epoxy-modified polysiloxane and carbon black is dispersed in a coating of 15 to 20 μm. It was coated and heat cured at a temperature of 300 ° C. for 15 minutes. Table 3 shows the reasons for using a methyl polysiloxane that forms a three-dimensional network as the topcoat.
【表3】 評価に下塗り層Fを用い、メチルポリシロキサンは例え
ば信越化学工業社製KR−220、メチルフェニルポリ
シロキサンは例えば信越化学工業社製メチル基60MO
L%とフェニル基40MOL%からなるポリシロキサン
KR−282、エポキシ変性ポリシロキサンは東芝シリ
コーン社製TSR−194、ポリエステル変性ポリシロ
キサンは東芝シリコーン社製TSR−187の単品また
は混合物それぞれに、珪酸マグネシウム例えば堀クレー
社製とカーボンブラック例えば三菱化成社製と直鎖状の
反応性ポリシロキサンは反応性ジメチルポリシロキサン
例えば東芝シリコーン社製YF−3800、珪酸マグネ
シウム及びカーボンブラックを混合分散した混合物を、
被膜で15〜20μmに被覆し、300℃の温度15分
間で加熱硬化を行なった。表4はメチルポリシロキサン
に与える鱗片顔料の効果を示す。[Table 3] The undercoat layer F was used for the evaluation, methyl polysiloxane was, for example, Shin-Etsu Chemical Co., Ltd. KR-220, and methylphenyl polysiloxane was, for example, Shin-Etsu Chemical Co., Ltd. methyl group 60MO.
Polysiloxane KR-282 composed of L% and phenyl group 40 MOL%, epoxy-modified polysiloxane is TSR-194 manufactured by Toshiba Silicone Co., Ltd., polyester-modified polysiloxane is TSR-187 manufactured by Toshiba Silicone Co., Ltd., individually or in a mixture, and magnesium silicate, for example, Hori Clay Co., Ltd. and carbon black, for example, Mitsubishi Kasei Co., Ltd. and linear reactive polysiloxane are reactive dimethyl polysiloxanes such as Toshiba Silicone Co. YF-3800, magnesium silicate and carbon black.
The coating was applied to a thickness of 15 to 20 μm, and heat-cured at a temperature of 300 ° C. for 15 minutes. Table 4 shows the effect of scale pigments on methyl polysiloxane.
【表4】 メチルポリシロキサンにおける鱗片顔料の効果確認につ
いての条件は、それぞれ上塗り層No1は珪酸マグネシ
ウム、No9は珪酸アルミニウム、No10は珪石粉、
No11は硫酸バリウム、No12は鱗片状金属酸化
物、No13は黒鉛、それぞれの単品に、メチルポリシ
ロキサンとカーボンブラックと直鎖状の反応性ポリシロ
キサンを混合分散した混合物を、またNo14〜No1
7はメチルポリシロキサンと珪酸マグネシウムの混合比
を変えカーボンブラックと直鎖状の反応性ポリシロキサ
ンを混合分散した混合物を、鉄素材へ、下塗り層Fを5
〜10μm、上塗り層を5〜10μmになるよう、二重
に被覆し、300℃の温度15分間で加熱硬化を行なっ
た。表5に直鎖状の反応性ポリシロキサンの効果を示
す。[Table 4] The conditions for confirming the effect of the scale pigments in methylpolysiloxane are as follows: Topcoat layer No. 1 is magnesium silicate, No. 9 is aluminum silicate, No. 10 is silica stone powder,
No. 11 is barium sulfate, No. 12 is scale-like metal oxide, No. 13 is graphite, and a mixture of methyl polysiloxane, carbon black and linear reactive polysiloxane is dispersed in each of the individual products, and No. 14 to No. 1
7 is a mixture of carbon black and linear reactive polysiloxane mixed and dispersed in which the mixing ratio of methylpolysiloxane and magnesium silicate is changed, and the undercoat layer F is coated with 5
-10 μm, the overcoat layer was double coated to 5 to 10 μm, and heat-cured at a temperature of 300 ° C. for 15 minutes. Table 5 shows the effect of the linear reactive polysiloxane.
【表5】 評価の汚染条件は、醤油と砂糖(2:1)の混合液を被
膜に滴化し、各温度で1時間の加熱を行い、固化させた
汚染物の取れ具合を○印はきれいに取れた、×は数回ス
コッチタワシで強く擦ると取れた、の結果を○×でつけ
た。直鎖状の反応性ポリシロキサンの評価に、下塗り層
Fを用い、非反応性ジメチルポリシロキサンは例えば信
越化学工業社製KF−96、反応性ジメチルポリシロキ
サンは例えば東芝シリコーン社製YF3800、非反応
性メチルフェニルポリシロキサンは例えば東芝シリコー
ン社製TSF437、反応性メチルフェニルポリシロキ
サンは例えば東芝シリコーン社製YF3804、アミノ
変性ポリシロキサンは例えば東芝シリコーン社製TSF
4700、エポキシ変性ポリシロキサンは例えば東芝シ
リコーン社製YF3965、ポリエーテル変性ポリシロ
キサンは例えば東芝シリコーン社製TSF4440、ま
たはアルキル変性ポリシロキサンは例えば東芝シリコー
ン社製TSF4421、単品のそれぞれに、三次元網目
状構造のメチルポリシロキサン、珪酸マグネシウム及び
カーボンブラックを混合分散した混合物を、鉄素材へ、
下塗り層Fを5〜10μm、上塗り層を5〜10μmに
なるよう、二重に被覆し、300℃の温度で15分間で
加熱硬化を行なった。表6に 加熱硬化条件と汚染性効
果を示す。[Table 5] The contamination condition of the evaluation is that a mixed solution of soy sauce and sugar (2: 1) was dropped on the film, heated at each temperature for 1 hour, and the solid contaminants were removed in a good manner. It was removed by rubbing it several times with a scotch scrubbing brush. For the evaluation of the linear reactive polysiloxane, the undercoat layer F was used. For the non-reactive dimethyl polysiloxane, for example, KF-96 manufactured by Shin-Etsu Chemical Co., Ltd., and for the reactive dimethyl polysiloxane, for example, YF3800 manufactured by Toshiba Silicone, non-reacted. The reactive methylphenyl polysiloxane is, for example, TSF437 manufactured by Toshiba Silicone, the reactive methylphenyl polysiloxane is, for example, YF3804 manufactured by Toshiba Silicone, and the amino-modified polysiloxane is, for example, TSF manufactured by Toshiba Silicone.
4700, an epoxy-modified polysiloxane is, for example, YF3965 manufactured by Toshiba Silicone, a polyether-modified polysiloxane is, for example, TSF4440 manufactured by Toshiba Silicone, or an alkyl-modified polysiloxane is, for example, TSF4421 manufactured by Toshiba Silicone, each of which is a three-dimensional network structure. The mixture of methyl polysiloxane, magnesium silicate and carbon black of
The undercoat layer F was doubly coated so as to have a thickness of 5 to 10 μm and the overcoat layer had a thickness of 5 to 10 μm, and heat-cured at a temperature of 300 ° C. for 15 minutes. Table 6 shows the heat curing conditions and the effect of contamination.
【表6】 評価の汚染性条件は、醤油と砂糖(2:1)の混合液を
被膜に滴化し、250℃の温度で1時間の加熱を行い、
固化させた汚染物を1時間自然冷却し、中性洗剤をスポ
ンジタワシにて汚れを落すという条件で、1サイクル、
10サイクル、50サイクル行い、その取れ具合を○印
はきれいに取れた、×は強く擦らないと取れない、と判
定しその結果を○×でつけた。耐熱耐汚染性被膜材の評
価に、ガステーブル部材の汁受皿5を用い、加熱硬化条
件と汚染性を下塗り層Fを10〜15μm、上塗り層1
を5〜10μmになるよう、二重に被覆し、180〜4
80℃の温度で15分間で加熱硬化を行なった。本発明
で耐熱被覆材として使用される三次元網目状構造を形成
するメチル基またはメチル基及びフェニル基からなるポ
リシロキサンの単品もしくはこれらの混合物は加熱によ
る減量は少なく硬質皮膜を形成し、また直鎖状の反応性
ポリシロキサンは側鎖または末端、或いは側鎖両末端に
反応基を有するもので、メチルポリシロキサンまたはメ
チルフェニルポリシロキサンと結合することにより、耐
熱性を有し汚染物が除去しやすい表面を形成出来るが、
そのままでは鉄素材である普通鋼材等の金属素地への密
着性が悪く、特に表面処理をしない素材を用いた場合、
加熱による変化で皮膜が剥離するという欠点があった。
前記、下塗リ層の変性ポリシロキサンは、シロキサン結
合の珪素原子に結合した水素基やメトキシ基をアルキド
樹脂、ポリエステル樹脂、アクリル樹脂またはエポキシ
樹脂等と反応させて得られるもの及びポリシロキサンと
これらの有機樹脂との混合によって得られるもの、或い
はシロキサン結合の珪素原子に結合する有機基がメチル
基やフェニル基で構成されるメチルフェニルポリシロキ
サンであり、素材への密着性及び硬化性に於いて好まし
くは有機基がエポキシ樹脂で変性されたポリシロキサン
をいう。また、上塗り層の三次元網目状構造を形成する
ポリシロキサンは、シロキサン結合の珪素原子に結合す
る有機基がメチル基とフェニル基からなるもので、好ま
しくはすべてメチル基で占められ末端には水酸基を有す
る構造のものである。この様に有機基がメチル基70%
以上であることによりフェニル基30%以上のポリシロ
キサンやアルキッドまたはエポキシ等で変性されたもの
に比べると加熱時の加熱減量劣化が少なく、被膜表面の
平滑性や特性が保持される。さらに、珪素原子に結合す
る有機基の数は少ない方が架橋密度が大きくなり硬化性
が高く被膜強度も強いため、有機基がメチル基であり、
かつ2官性能もしくは3官性能のメチルポリシロキサン
である。直鎖状の反応性ポリシロキサンとは、側鎖、末
端或いは側鎖両端末に反応機を有するもので、メチルポ
リシロキサンと結合して表面に汚染物の除去を容易にす
る強い被膜を形成し、ポリシロキサンの持つ対汚染性と
汚染物の除去の容易性を永続的に与える特徴が得られ
る。非反応性のメチル基またはフェニル基を結合するポ
リシロキサンも対汚染性と汚染物の除去の容易性を有し
ているが、被膜表面にポリシロキサン層が形成されてい
るだけで、繰返しの使用により次第に表面層から離脱し
て長期の使用には耐えない。鱗片状構造を持つ珪酸マグ
ネシウム、珪酸アルミニウムの珪酸塩化合物、金属酸化
物顔料、黒鉛の中から選ばれる、厚さ10μm以下でア
スペクト比0.1〜15の鱗片状物質の単品もしくは、
これらの混合物は被膜のひび割れ防止や柔軟性を向上さ
せ、永続性がある。また上塗り層に色彩美観をもたせる
場合は、着色材や擦り防止用の四フッ化エチレン樹脂
等、公知の材料を被覆材に混入することが出来、さらに
添加剤として硬化剤を併用することによって、低温短時
間の加熱硬化が図れる。このことは下塗り層も同様であ
り、これら不揮発成分の被覆を均一に塗布するため、揮
発成分である芳香族炭化水素、、アルコール、ケトン、
その他の有機溶剤の単品もしくは混合溶剤に分散させ、
ガステーブル部材であるグリル部2、トッププレート
3、汁受皿5に乾燥後の膜厚として8〜150μm(下
塗り層3〜70μm、上塗り層5〜80μm)になるよ
う塗布し、塗布後200〜450℃の温度で10〜30
分間加熱硬化させることによって、調理物から出た汁や
油のこびり付きをなくした。[Table 6] The contamination condition of the evaluation is as follows: a mixed solution of soy sauce and sugar (2: 1) is dropped on the film and heated at a temperature of 250 ° C. for 1 hour.
One cycle under the condition that the solidified contaminants are naturally cooled for 1 hour and the neutral detergent is removed with a sponge scrubbing brush,
The test was performed 10 cycles and 50 cycles, and it was judged that the O marks could be taken cleanly and the X marks could not be taken without strong rubbing. In the evaluation of the heat-resistant and stain-resistant coating material, the juice tray 5 of the gas table member was used.
Is double-coated so as to be 5 to 10 μm, and 180 to 4
Heat curing was carried out at a temperature of 80 ° C. for 15 minutes. The polysiloxane alone or a mixture thereof containing a methyl group or a methyl group and a phenyl group forming a three-dimensional network structure used as a heat-resistant coating material in the present invention forms a hard film with little weight loss due to heating, and also has a direct coating. The chain-like reactive polysiloxane has a reactive group at the side chain or at the terminal, or at both ends of the side chain. By combining with methylpolysiloxane or methylphenylpolysiloxane, it has heat resistance and removes contaminants. It can form an easy surface,
As it is, the adhesion to the metal base such as ordinary steel which is an iron material is poor, especially when using a material that is not surface treated,
There was a drawback that the film peeled off due to changes due to heating.
The modified polysiloxane of the undercoat layer is obtained by reacting a hydrogen group or a methoxy group bonded to a silicon atom of a siloxane bond with an alkyd resin, a polyester resin, an acrylic resin or an epoxy resin, and polysiloxane and these A compound obtained by mixing with an organic resin, or methylphenylpolysiloxane in which the organic group bonded to the silicon atom of the siloxane bond is a methyl group or a phenyl group, and is preferable in terms of adhesion to materials and curability. Represents a polysiloxane whose organic group is modified with an epoxy resin. Further, the polysiloxane forming the three-dimensional network structure of the overcoat layer is one in which the organic group bonded to the silicon atom of the siloxane bond is composed of a methyl group and a phenyl group, and preferably all are occupied by a methyl group and a hydroxyl group at the end. The structure has In this way, the organic group is 70% methyl group
As a result of the above, compared to those modified with polysiloxane having 30% or more of phenyl groups, alkyd, epoxy or the like, the loss on heating loss during heating is less, and the smoothness and characteristics of the coating surface are maintained. Furthermore, the smaller the number of organic groups bonded to silicon atoms, the higher the crosslink density, the higher the curability and the higher the film strength, so the organic groups are methyl groups,
It is a methylpolysiloxane with two or three performances. A linear reactive polysiloxane has a reactor at the side chain, terminal or both ends of the side chain, and forms a strong coating on the surface that combines with methyl polysiloxane to facilitate the removal of contaminants. , A characteristic that permanently imparts the anti-contamination property of polysiloxane and the ease of removing the contaminant is obtained. Non-reactive methyl group- or phenyl group-bonded polysiloxanes also have anti-contamination properties and easy removal of contaminants, but only a polysiloxane layer is formed on the surface of the film, and repeated use is possible. As a result, it gradually disengages from the surface layer and cannot withstand long-term use. A single scale-like substance having a thickness of 10 μm or less and an aspect ratio of 0.1 to 15 selected from magnesium silicate having a scale-like structure, a silicate compound of aluminum silicate, a metal oxide pigment, and graphite, or
These mixtures improve the crack resistance and flexibility of the coating and are durable. When the topcoat layer has a color appearance, known materials such as a colorant and a tetrafluoroethylene resin for rubbing prevention can be mixed with the coating material, and by further using a curing agent as an additive, Heat curing at low temperature for a short time can be achieved. This is the same in the undercoat layer, in order to uniformly coat the coating of these non-volatile components, aromatic hydrocarbons, which are volatile components, alcohol, ketone,
Disperse in other organic solvent alone or mixed solvent,
It is applied to the grill part 2, the top plate 3, and the soup saucer 5 which are gas table members so as to have a film thickness after drying of 8 to 150 μm (undercoat layer 3 to 70 μm, topcoat layer 5 to 80 μm), and 200 to 450 after application. 10 to 30 at a temperature of ℃
By heating and curing for minutes, the stickiness of juice and oil from the cooked food was eliminated.
【発明の効果】以上のように本発明は、調理器具のトッ
ププレート、汁受皿やグリルの庫内等に、変性ポリシロ
キサン及び鱗片状構造を持つ珪酸マグネシウム、珪酸ア
ルミニウムの珪酸塩化合物、鱗片状金属酸化鉄顔料、黒
鉛の単品もしくはこれらの混合物を主成分とする下塗り
層と、三次元網目状構造を形成するメチル基またはメチ
ル基及びフェニル基を含有したポリシロキサンと直鎖状
の反応性ポリシロキサン及び鱗片状構造を持つ珪酸マグ
ネシウム、珪酸アルミニウムの珪酸塩化合物、鱗片状金
属酸化鉄顔料、黒鉛の単品もしくはこれらの混合物を主
成分とする被覆材を上塗り層として加熱硬化させた二重
構造からなる耐熱耐汚染性被膜被覆を施したから、被膜
の柔軟性、密着性が向上し、ひび割れ防止や永続性を持
たせる効果があり、調理物から出た汁や油のこびり付き
の少ない、清掃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。INDUSTRIAL APPLICABILITY As described above, according to the present invention, the modified polysiloxane and the magnesium silicate having a scaly structure, the silicate compound of aluminum silicate, and the scaly form are used in the top plate of the cooking utensil, the soup saucer and the inside of the grill. An undercoat layer composed mainly of a metallic iron oxide pigment, a single piece of graphite or a mixture thereof, a polysiloxane containing a methyl group or a methyl group and a phenyl group forming a three-dimensional network structure and a linear reactive poly From a double structure in which siloxane and magnesium silicate having a scaly structure, a silicate compound of aluminum silicate, a scaly metal iron oxide pigment, a single graphite product or a mixture of these as a main component is heat-cured as an overcoat layer. Since it is coated with a heat-resistant and stain-resistant coating, it has the effects of improving the flexibility and adhesion of the coating, preventing cracks, and providing durability. Less sticking of juice and oil exiting from the food, in which it is possible to provide an excellent cookware cleanability.
【図1】本発明に係る調理器具を示すガステーブルの一
部分解斜視図である。FIG. 1 is a partially exploded perspective view of a gas table showing a cooking utensil according to the present invention.
【図2】本発明に係る調理器具を示すオーブンレンジの
斜視図である。FIG. 2 is a perspective view of a microwave oven showing a cooking utensil according to the present invention.
2 グリル部 3 トッププレート 5 汁受皿 9 調理庫 2 Grill part 3 Top plate 5 Soup saucer 9 Cooking room
───────────────────────────────────────────────────── フロントページの続き (72)発明者 豊永 隆 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 尾家 孝志 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 Takashi Toyonaga 1109, Shibaide, Kuramochi-cho, Nabari-shi, Mie Prefecture Okitsumo Co., Ltd. (72) Takashi Oie, 1109, Shibaide, Kuramochi-cho, Nabari-shi, Mie Tsumo Co., Ltd.
Claims (3)
る調理器具において、調理によって汚れが付着するグリ
ル部(2)、トッププレート(3)、汁受皿(5)、調
理庫(9)に変性ポリシロキサン及び鱗片状構造を持つ
珪酸マグネシウム、珪酸アルミニウムの珪酸塩化合物、
鱗片状金属酸化鉄顔料、黒鉛の単品もしくはこれらの混
合物を主成分とする被覆材を下塗り層とし、三次元網目
状構造を形成するメチル基またはメチル基及びフェニル
基を含有したポリシロキサンと直鎖状の反応性ポリシロ
キサン及び鱗片状構造を持つ珪酸マグネシウム、珪酸ア
ルミニウムの珪酸塩化合物、鱗片状金属酸化鉄顔料、黒
鉛の単品もしくはこれらの混合物を主成分とする被覆材
を上塗り層として加熱硬化させた二重構造からなる耐熱
耐汚染性被膜被覆を施した調理器具。1. In a cooking utensil for heating and cooking food such as a gas table, a grill part (2), a top plate (3), a soup saucer (5), and a cooking cabinet (9) to which dirt adheres due to cooking. Modified polysiloxane and scale-like magnesium silicate, aluminum silicate silicate compound,
Scaly metal iron oxide pigments, graphite alone or a coating material mainly composed of a mixture thereof as an undercoat layer, and a polysiloxane containing a methyl group or a methyl group and a phenyl group forming a three-dimensional network structure and a straight chain -Like reactive polysiloxane and scale-like magnesium silicate, aluminum silicate silicate compound, scale-like iron oxide iron pigment, graphite single substance or a coating material containing a mixture thereof as a main component is heat-cured as an overcoat layer. Cookware with heat resistant and stain resistant coating with double structure.
の下塗り層は変性ポリシロキサン及び鱗片状構造を持つ
珪酸マグネシウム、珪酸アルミニウムの珪酸塩化合物、
鱗片状金属酸化鉄顔料、黒鉛の中から選ばれる厚さ10
μm以下でアスペクト比0.1〜15の鱗片状物質の単
品もしくはこれらの混合物5〜50重量部を主成分と
し、着色材、増量材が0〜40重量部の割合で含む混合
物でなり、また、上塗り層は三次元網目状構造を形成す
るメチル基70〜100MOL%、フェニル基0〜30
MOL%からなるポリシロキサンの単品もしくはこれら
の混合物で50〜99重量部及び直鎖状の反応性ポリシ
ロキサン1〜20重量部と、鱗片状構造を持つ珪酸マグ
ネシウム、珪酸アルミニウムの珪酸塩化合物、鱗片状金
属酸化鉄顔料、黒鉛の中から選ばれる厚さ10μm以下
でアスペクト比0.1〜15の鱗片状物質の単品もしく
はこれらの混合物5〜30重量部を主成分とし、着色
材、増量材が0〜60重量部の割合で含む混合物でなる
ものとしたことを特徴とする請求項1記載の調理器具の
汚染防止被覆材。2. An undercoat layer having a double-structured heat and stain resistant coating is a modified polysiloxane and a silicate compound of magnesium silicate or aluminum silicate having a scaly structure.
Flake-shaped metallic iron oxide pigment, thickness selected from graphite 10
It is a mixture containing 5 to 50 parts by weight of a scaly substance having an aspect ratio of 0.1 to 15 and a mixture of 5 to 50 parts by weight as a main component, and a colorant and an extender in a ratio of 0 to 40 parts by weight. The overcoat layer is a methyl group 70-100 MOL% and a phenyl group 0-30 forming a three-dimensional network structure.
50 to 99 parts by weight of a polysiloxane consisting of MOL% or a mixture thereof, and 1 to 20 parts by weight of a linear reactive polysiloxane, magnesium silicate having a scaly structure, a silicate compound of aluminum silicate, and a scale. Metallic iron oxide pigments, graphite having a thickness of 10 μm or less and an aspect ratio of 0.1 to 15 and a scale-like substance alone or 5 to 30 parts by weight of a mixture thereof as a main component. The anti-contamination coating material for cookware according to claim 1, wherein the coating material is a mixture containing 0 to 60 parts by weight.
材は、下塗り層が乾燥膜厚で3〜70μm、上塗り層は
乾燥膜厚で5〜80μmに仕上がるように塗装し、20
0〜450℃の温度で10〜30分間の加熱乾燥して被
覆化したことを特徴とする請求項1記載の調理器具又は
請求項2記載の調理器具の汚染防止被覆材の塗装方法。3. A heat- and stain-resistant coating material having a double structure is applied so that the undercoat layer has a dry film thickness of 3 to 70 μm and the overcoat layer has a dry film thickness of 5 to 80 μm.
The coating method of the cooking utensil according to claim 1 or the anti-contamination coating material of the cooking utensil according to claim 2, characterized by coating by heating and drying at a temperature of 0 to 450 ° C for 10 to 30 minutes.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29697892A JPH06147502A (en) | 1992-11-06 | 1992-11-06 | Cooker, contaminant preventing cover material and painting method thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP29697892A JPH06147502A (en) | 1992-11-06 | 1992-11-06 | Cooker, contaminant preventing cover material and painting method thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH06147502A true JPH06147502A (en) | 1994-05-27 |
Family
ID=17840670
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP29697892A Pending JPH06147502A (en) | 1992-11-06 | 1992-11-06 | Cooker, contaminant preventing cover material and painting method thereof |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH06147502A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3531026B1 (en) | 2009-07-15 | 2021-10-20 | LG Electronics Inc. | Cooker |
-
1992
- 1992-11-06 JP JP29697892A patent/JPH06147502A/en active Pending
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3531026B1 (en) | 2009-07-15 | 2021-10-20 | LG Electronics Inc. | Cooker |
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