JPH0338254A - Heat-resisting film - Google Patents

Heat-resisting film

Info

Publication number
JPH0338254A
JPH0338254A JP1172214A JP17221489A JPH0338254A JP H0338254 A JPH0338254 A JP H0338254A JP 1172214 A JP1172214 A JP 1172214A JP 17221489 A JP17221489 A JP 17221489A JP H0338254 A JPH0338254 A JP H0338254A
Authority
JP
Japan
Prior art keywords
film
heat
oil
binder
tar
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
Application number
JP1172214A
Other languages
Japanese (ja)
Inventor
Makiko Waki
脇 真起子
Yasunori Kaneko
金子 康典
Akio Fukuda
明雄 福田
Mamoru Isoya
守 礒谷
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP1172214A priority Critical patent/JPH0338254A/en
Publication of JPH0338254A publication Critical patent/JPH0338254A/en
Pending legal-status Critical Current

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  • Baking, Grill, Roasting (AREA)
  • Cookers (AREA)
  • Catalysts (AREA)

Abstract

PURPOSE:To obtain a film which provides so a hard and slippery surface as to permit the removal of oily stains by mixing a layer structure compound and a solid oxide compound with polyporosiloxane for use as a binder. CONSTITUTION:Semiorganic polyporosiloxane and polyporotitanosiloxane are used as a binder in the formation of a heat-resisting film on the surface of the inner wall of cooking oven, grille, etc. A layer structure compound such as quartz glass is mixed with such film to make it flat and smooth and a solid oxide compound such as ZrO2 is also mixed therewith to control the formation of tar. Since the film thus formed is high in solidity, good in surface slipperiness and has a cracking action on oily stains, the soiled spots are easy to remove.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は調理用オーブン、グリル等の庫内壁面のように
油汚れの目立つ部分に適用する油汚れの浄化能力を持つ
耐熱性被膜に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a heat-resistant coating that has the ability to purify oil stains and is applied to areas where oil stains are noticeable, such as the inner walls of cooking ovens, grills, etc. .

従来の技術 従来、油汚れを触媒燃焼させて除去する能力を持つ被膜
については、金属のリン酸塩やケイ酸塩等の耐熟性無機
バインダー中にMn、Cu、Fe。
BACKGROUND OF THE INVENTION Conventionally, coatings with the ability to remove oil stains by catalytic combustion have been developed using Mn, Cu, and Fe in a ripening-resistant inorganic binder such as a metal phosphate or silicate.

Co、Ni等の各金属酸化物か、もしくは各金属酸化物
の混合物や複合物を分散したものが殆んどであった。
Most of the materials were dispersed with metal oxides such as Co and Ni, or mixtures or composites of metal oxides.

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 uses 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類題がある
Problems to be Solved by the Invention However, the above conventional techniques have similar problems as follows.

1ず第1に、油汚れを完全燃焼させるためには。1. First of all, to completely burn off the oil stains.

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
するために被膜をできるだけ多孔質にしなければならな
い。しかし多孔質にすると硬度が低くなシ剥離したシ傷
ついたシし実用上問題がある。
The coating must be made as porous as possible in order to increase the contact area between the oil and the catalyst and improve oxygen diffusion within the coating. However, if it is made porous, the hardness is low, and there are practical problems such as peeling and scratches.

筐た焼は残ったタール成分が多孔質の隙間に入シ込んで
沈着してし!い、浄化性能が徐々に低下する可能性があ
る。
In Kakitayaki, the remaining tar components get into the porous gaps and settle! However, the purification performance may gradually decrease.

第2に、油が燃焼する際には局部的に温度がs o O
”C位壕で上がるため、金属酸化物が徐々に焼結し浄化
性能が低下したう、筐た金属酸化物の還元により被膜が
変色したシする。
Second, when oil burns, the local temperature is s o O
``As the C level rises in the trenches, the metal oxide gradually sinters, reducing purification performance, and the coating changes color due to reduction of the metal oxide in the casing.

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方
法を取り上げる。
As mentioned above, there are some problems with the conventional technology, but the present invention deals with a method of cleaning oil stains on a dense and highly hard film.

課題を解決するための手段 上記課題を解決するために、本発明はポリボロシロキサ
ン、ポリボロ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鴎造を持つ化合物と固体酸化
合物とからなるものである。
Means for Solving the Problems In order to solve the above problems, the present invention provides a method using a compound having a layered structure and a solid acid compound using one or a mixture of the two of polyborosiloxane and polyborotitanosiloxane as a binder. It is what it is.

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.

R,−C−0−CH2 1 (R1,R2、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か起こる。
R, -C-0-CH2 1 (R1, R2, Rs are saturated or 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460°C以上の高温が要
求される。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。
High temperatures of 460°C or higher are required to oxidize and decompose tar. 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 ability to purify dirt.

そこで本発明では1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, in the present invention, first of all, we focused 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質であるポリボ
ロシロキサン、ポリボロチタノシロキサンは450″C
以上で焼成すると無機質化して非常に緻密な薄膜を形成
することができる。
The semi-organic polyborosiloxane and polyborotitanosiloxane used as the binder in the present invention have a temperature of 450"C.
When fired in the above manner, it becomes mineralized and a very dense thin film can be formed.

更に層状化合物を混入することにより被膜表面を平滑に
し滑り性をよくした。
Furthermore, by mixing a layered compound, the surface of the coating was smoothed and smoothness was improved.

また被膜表面が非酸化物層であるためタール成分の化学
的吸着力も弱い。従って加熱下で生成したタールは簡単
に被膜表面から剥離する。被膜が平滑であるため剥離し
たタール成分やその他の汚れは簡単にふき取ることがで
きる。
Furthermore, since the coating surface is a non-oxide layer, the chemical adsorption power of tar components is also weak. Therefore, the tar generated under heating is easily peeled off from the coating surface. Since the film is smooth, peeled tar components and other dirt can be easily wiped off.

第2にタール生成を抑制するために固体酸を添加した。Second, solid acid was added to suppress tar formation.

固体酸の作用により’amの表層部分で油の炭素間結合
を切断し空気中の酸素にょシ二酸化炭素筐で分解させる
ものである。
The action of solid acid breaks the carbon-carbon bonds in the oil at the surface of the 'am, causing it to decompose in the oxygen and carbon dioxide chambers in the air.

以上のように本発明の耐熱性被膜は、固体酸の作用で油
汚れを酸化分解し、更にm膜が緻密で表面の滑シ性がよ
いために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。
As described above, the heat-resistant coating of the present invention oxidizes and decomposes oil stains through the action of solid acids, and furthermore, because the m-film is dense and has good surface lubricity, residual tar components and ash are easily removed. Peel off,
It is possible to wipe it off.

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.

璽ず製法について説明する。バインダーとフィラー、固
体酸化合物や硫化物もしくは窒化物と溶剤を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。
I will explain the method of making jizu. Binder and filler, solid acid compound, sulfide or nitride and solvent for 24 hours,
Disperse the paint with an attritor and spray it with a spray gun (DeVilbiss spray gun).

/x’ルロ径1.4tilφ、 Air圧2〜2.5 
kg /cd )でステンレス(St)8304,43
0)基材上に塗布し100″C→SOO°Cで順に焼成
して被膜を作成した。
/x' Roulo diameter 1.4tilφ, Air pressure 2~2.5
kg/cd) stainless steel (St) 8304,43
0) A film was created by coating on a substrate and baking in order at 100''C→SOO°C.

次に被膜上に一定量のサラダ油を滴下し、一定温度に設
定したオープ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 open at a certain temperature to perform 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1とめ第1表に示した。配合はすべて重量比で示し
た。
Table 1 shows the composition of the paint used to form the film and the results of the oil purification test. All formulations are shown in weight ratios.

(以 下 余 白) 尚、溶剤としてトルエンを180の割合で加えた。(Hereafter, extra white) Note that toluene was added as a solvent at a ratio of 180:1.

/161〜10については他に石英ガラスを10.ホー
ロー成分を20の割合で添加し、贋11及び涜12につ
いては石英ガラスを10添加しである。
For /161-10, quartz glass is also used. The enamel component was added at a ratio of 20 parts, and for fakes 11 and 12, 10 parts of quartz glass was added.

油浄化テストは380°Cで行い、浄化に要した時間を
示した。
The oil purification test was conducted at 380°C and the time required for purification was indicated.

今回1石英ガラスを添加したのは膜硬度を上げるためで
ある。またMoS2. WS2. B Nを添加しノく
インダーとしてポリボロシロキサンを用いた涜1〜/1
69の膜は滑り性がよ(410−AI 2(7)膜は多
孔質に仕上がっていた。MoS2. WS2. B N
の中ではMoS2を添加した膜が鉛筆硬度9Hと非常に
高い硬度を示した。
The reason why 1 quartz glass was added this time was to increase the film hardness. Also MoS2. WS2. BN addition and using polyborosiloxane as an inder 1~/1
The membrane of No. 69 has good slipperiness (410-AI 2 (7) membrane has a porous finish. MoS2. WS2. B N
Among these, the film containing MoS2 had a very high pencil hardness of 9H.

固体酸については酸強度が5in2/ムe2o、>zr
o2) TiO2であるためTiO2を添加した/% 
7 。
For solid acids, the acid strength is 5in2/mu e2o, >zr
o2) Since it is TiO2, TiO2 was added/%
7.

8.9は多少浄化性能が釦とる。しかし今回用いりSi
O2/ムe20.(ZSM−s)ハ酸強IIカ強スキて
油の浄化テストの途中で膜がボロボロと剥離した。今回
用いた固体酸の中ではZr02(神戸製鋼■R5C−1
00)が最適である。
8.9 has somewhat better purification performance. However, this time we used Si
O2/mu e20. (ZSM-s) The membrane peeled off during the oil purification test using strong halogen acid II. Among the solid acids used this time, Zr02 (Kobe Steel R5C-1
00) is optimal.

油浄化テストの結果、第1表かられかるように41〜/
166については約380’C,約2.5 hr、で分
解除去してし捷う。また涜1は膜硬度が9Hと高く、緻
密で滑り性があり浄化性能の高い膜となり、酸で炭素間
結合を切断し、硫化物あるいは窒化物で膜表面とタール
の結合力を弱めることができた。
The results of the oil purification test were 41~/ as shown in Table 1.
166 is decomposed and removed at about 380'C for about 2.5 hours. In addition, Fukui 1 has a high film hardness of 9H, resulting in a dense and slippery film with high purification performance.It is possible to break carbon-carbon bonds with acid and weaken the binding force between the film surface and tar with sulfides or nitrides. did it.

A10のように金属酸化物を添加した場合は。When metal oxide is added like A10.

金属酸化物がバインダーに覆われてし筐い、酸素雰囲気
下で油を燃焼させることができず残渣が残った。
The metal oxides were covered with binder and the oil could not be burned in an oxygen atmosphere, leaving a residue.

筐たリン酸塩やケイ酸塩をバインダーとして用いた/1
610,11は、膜のpHが酸あるいはアルカリに片寄
るため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。
Using a cased phosphate or silicate as a binder/1
No. 610 and No. 11 had poor oil purification performance because the pH of the membrane was biased toward acid or alkali, and because they were porous, tar was deposited inside the pores.

以上のように本発明の耐熱性被膜は汚れの持つ炭素間結
合を切断し、更に被膜表面とタールとの結合力を物理的
・化学的に弱めることができるため調理器庫内壁面等の
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 break the carbon-carbon bonds of dirt and physically and chemically weaken the bonding force between the coating surface and tar, so it can be used in practical applications such as on the inner walls of cooking appliances. It is a heat-resistant coating suitable for

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1
表面の滑り性が良好であり、更に油汚れのクラ、−、キ
ング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 detail, the heat-resistant coating of the present invention has a high hardness of 1.
Since the surface has good slipperiness and also has a cleaning effect on oil stains, it is possible to obtain a coating that is excellent in cleaning stains inside the cooker.

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被膜をいつ1でもきれいな
状態に保つことができる。
After dirt adheres to the film, the dirt is removed by heating the film, and the remaining ash and deposits can be easily peeled off and wiped off, so the film can be kept in a clean state at all times.

Claims (3)

【特許請求の範囲】[Claims] (1)ポリボロシロキサン、ポリボロチタノシロキサン
の1種もしくは2種の混合物をバインダーとし、層状構
造を持つ化合物と固体酸化合物からなる耐熱性被膜。
(1) A heat-resistant film made of a compound having a layered structure and a solid acid compound, using one or a mixture of the two of polyborosiloxane and polyborotitanosiloxane as a binder.
(2)層状構造を持つ化合物は、MoS_2、WS_2
、BNの1種もしくは2種以上の混合物から成る特許請
求の範囲第1項記載の耐熱性被膜。
(2) Compounds with layered structure are MoS_2, WS_2
, BN or a mixture of two or more thereof.
(3)固体酸化合物がZrO_2、TiO_2、SiO
_2−Al_2O_3の1種もしくは2種以上の混合物
から成る特許請求の範囲第1項記載の耐熱性被膜。
(3) Solid acid compounds are ZrO_2, TiO_2, SiO
The heat-resistant coating according to claim 1, comprising one type or a mixture of two or more types of _2-Al_2O_3.
JP1172214A 1989-07-04 1989-07-04 Heat-resisting film Pending JPH0338254A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1172214A JPH0338254A (en) 1989-07-04 1989-07-04 Heat-resisting film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1172214A JPH0338254A (en) 1989-07-04 1989-07-04 Heat-resisting film

Publications (1)

Publication Number Publication Date
JPH0338254A true JPH0338254A (en) 1991-02-19

Family

ID=15937712

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1172214A Pending JPH0338254A (en) 1989-07-04 1989-07-04 Heat-resisting film

Country Status (1)

Country Link
JP (1) JPH0338254A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5370729A (en) * 1993-09-15 1994-12-06 Ecolab Inc. Food safe composition to facilitate soil removal
US5494503A (en) * 1995-02-16 1996-02-27 Ecolab Inc. Soil release coating for heat transfer surfaces
EP1486473A1 (en) 2003-06-13 2004-12-15 ESK Ceramics GmbH & Co.KG Durable mould release coatings for die casting of nonferrous metals comprising boron nitride
DE10127494B4 (en) * 2001-06-09 2005-07-07 Itn Nanovation Gmbh High temperature stable inorganic boron nitride layers
EP1386983B2 (en) 2002-07-31 2010-06-09 ItN NANOVATION GMBH Ceramic coating for a boiler

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5370729A (en) * 1993-09-15 1994-12-06 Ecolab Inc. Food safe composition to facilitate soil removal
US5407700A (en) * 1993-09-15 1995-04-18 Ecolab Inc. Food safe composition to facilitate soil removal
US5494503A (en) * 1995-02-16 1996-02-27 Ecolab Inc. Soil release coating for heat transfer surfaces
DE10127494B4 (en) * 2001-06-09 2005-07-07 Itn Nanovation Gmbh High temperature stable inorganic boron nitride layers
EP1386983B2 (en) 2002-07-31 2010-06-09 ItN NANOVATION GMBH Ceramic coating for a boiler
EP1486473A1 (en) 2003-06-13 2004-12-15 ESK Ceramics GmbH & Co.KG Durable mould release coatings for die casting of nonferrous metals comprising boron nitride
EP1486473B1 (en) * 2003-06-13 2007-09-05 ESK Ceramics GmbH & Co.KG Durable mould release coatings for die casting of nonferrous metals comprising boron nitride

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