JPS5949314B2 - How to prevent carbonaceous deposits on surfaces - Google Patents
How to prevent carbonaceous deposits on surfacesInfo
- Publication number
- JPS5949314B2 JPS5949314B2 JP14730179A JP14730179A JPS5949314B2 JP S5949314 B2 JPS5949314 B2 JP S5949314B2 JP 14730179 A JP14730179 A JP 14730179A JP 14730179 A JP14730179 A JP 14730179A JP S5949314 B2 JPS5949314 B2 JP S5949314B2
- Authority
- JP
- Japan
- Prior art keywords
- particle size
- oil
- carbonaceous deposits
- coating
- inorganic
- 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
Links
- 239000002245 particle Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 239000011247 coating layer Substances 0.000 claims description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 5
- 230000008021 deposition Effects 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims description 2
- 229910001463 metal phosphate Inorganic materials 0.000 claims description 2
- 238000000576 coating method Methods 0.000 description 11
- 239000003921 oil Substances 0.000 description 10
- 235000019198 oils Nutrition 0.000 description 10
- 238000007254 oxidation reaction Methods 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 230000003647 oxidation Effects 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 229910052809 inorganic oxide Inorganic materials 0.000 description 7
- 239000003973 paint Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 150000001875 compounds Chemical group 0.000 description 4
- 238000010411 cooking Methods 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 230000008020 evaporation Effects 0.000 description 4
- NUJOXMJBOLGQSY-UHFFFAOYSA-N manganese dioxide Chemical compound O=[Mn]=O NUJOXMJBOLGQSY-UHFFFAOYSA-N 0.000 description 4
- 239000002585 base Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000003350 kerosene Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000008016 vaporization Effects 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000002309 gasification Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 150000002894 organic compounds Chemical class 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 239000011973 solid acid Substances 0.000 description 2
- 238000009834 vaporization Methods 0.000 description 2
- FBOUIAKEJMZPQG-AWNIVKPZSA-N (1E)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-AWNIVKPZSA-N 0.000 description 1
- 229910000680 Aluminized steel Inorganic materials 0.000 description 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 description 1
- 239000005751 Copper oxide Substances 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- -1 ZnO2 Chemical compound 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical group 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical group 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- ILRRQNADMUWWFW-UHFFFAOYSA-K aluminium phosphate Chemical compound O1[Al]2OP1(=O)O2 ILRRQNADMUWWFW-UHFFFAOYSA-K 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000378 calcium silicate Chemical group 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical group [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- XFWJKVMFIVXPKK-UHFFFAOYSA-N calcium;oxido(oxo)alumane Chemical group [Ca+2].[O-][Al]=O.[O-][Al]=O XFWJKVMFIVXPKK-UHFFFAOYSA-N 0.000 description 1
- 239000003575 carbonaceous material Substances 0.000 description 1
- 238000003763 carbonization Methods 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000006356 dehydrogenation reaction Methods 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000002320 enamel (paints) Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 238000007750 plasma spraying Methods 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 235000012045 salad Nutrition 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
Landscapes
- Other Surface Treatments For Metallic Materials (AREA)
- Paints Or Removers (AREA)
Description
【発明の詳細な説明】
本発明はオープン等の調理器の庫内壁、あるいは気化式
灯油燃焼バーナの油気化面など、調理器残渣あるいは、
灯油の重合生成物であるタールなどの炭素質堆積が懸念
される表面において、その炭素質堆積を抑制し、更には
分解して除去することを目的とした表面上への炭素質堆
積を防止するための方法に関する提案である。DETAILED DESCRIPTION OF THE INVENTION The present invention can be used to remove cooking device residue or
On surfaces where carbonaceous deposits such as tar, which is a polymerization product of kerosene, are a concern, this method suppresses carbonaceous deposits and further prevents carbonaceous deposits on surfaces that are intended to be decomposed and removed. This is a proposal on how to do this.
料理用装置の庫内に適用して、食品等の汚れを触媒的に
浄化することを目的とした被覆表面に関する提案は、デ
ュポン社のスタイルズによつてなされ、以降同様の考え
方のもとに、酸化触媒を水ガラス系の結合剤ではなくガ
ラスフリット中へ分散させる方法などが相次いで提案さ
れ実用化されている。A proposal regarding a coated surface for the purpose of catalytically purifying food stains by applying it to the inside of cooking equipment was made by Stiles of DuPont, and has since been based on the same idea. , methods of dispersing oxidation catalysts in glass frit rather than in a water glass binder have been successively proposed and put into practical use.
これらの一連の提案の要旨は、油、脂肪酸、たん白質な
どの有機化合物を触媒的に酸化して浄化することであり
、有機化合物の完全酸化即ち燃焼を触媒を用いて200
〜300℃程度の低温で行なおうという考え方に基づく
ものである。本発明者らは、調理汚染物による表面の汚
染を防止するためには、従来から一般的に言われるとこ
ろの「酸化触媒」は真に有効かという点に疑問を感じ、
調理汚染物として、特に悪質な汚染をもたらす脂肪酸に
ついて、脂肪酸の炭素化の防止の観点から、触媒による
脂肪酸のガス化分解を追究した。その結果、アルカリ金
属、アルカリ土類金属などの酸化物や、ケイ酸カルシウ
ム、アルミン酸カルシウムその他の化合物群、あるいは
Ti、Fe、Ni、Co、Cr、Agなどの酸化物が優
れた触媒能力を持つていることを見出し既に提案した。The gist of these series of proposals is to catalytically oxidize and purify organic compounds such as oils, fatty acids, and proteins.
This is based on the idea that the process should be carried out at a low temperature of about 300°C. The inventors of the present invention have doubts about whether "oxidation catalysts," which have been commonly referred to in the past, are truly effective in preventing surface contamination by cooking contaminants.
Regarding fatty acids that cause particularly bad cooking contaminants, we investigated gasification and decomposition of fatty acids using catalysts from the viewpoint of preventing fatty acid carbonization. As a result, oxides such as alkali metals and alkaline earth metals, calcium silicate, calcium aluminate, and other compound groups, and oxides such as Ti, Fe, Ni, Co, Cr, and Ag have excellent catalytic abilities. I have already suggested that you have a heading.
この中で、従来から一般的に言われている「酸化触媒」
の中、二酸化マンガン、酸化銅などは、脂肪酸のガス化
分解能力に関しては、ほとんどoで、むしろ分解を阻止
していることなども見出した。本発明は、従来の「酸化
触媒」を用いたり、あるいは「ガス化分解触媒」を用い
たりする方法とは観点が全く異なり、別の浄化機構に基
づくものである。タールの堆積が問題となるのは、多く
の場合、炭化水素化合物がそこで相当量気化する物体の
表面であることが多い。Among these, "oxidation catalyst" which has been commonly referred to as
Among them, it was found that manganese dioxide, copper oxide, etc. had almost no ability to gasify and decompose fatty acids, but rather inhibited the decomposition. The present invention is completely different from the conventional method using an "oxidation catalyst" or a "gasification decomposition catalyst" and is based on a different purification mechanism. Tar deposits are often a problem on the surfaces of objects where hydrocarbon compounds are vaporized in significant amounts.
従来のセルフクリーニング被覆においては、「酸化触媒
」などを用いたりしてこれを積極的に酸化させたりする
訳であるが、本発明はその種の反応には頼らないもので
ある。物体表面からの蒸発、気化の促進が本発明の浄化
機構の全てである。従つて、表面被覆の構成は極めて単
純である。但し、肝要な点は、積極的な酸化作用を極力
押さえる点にある。この様な点が従来のセルフクリーニ
ング被覆などと基本的に異なる所である。本発明の方法
を具体的に行なう表面被覆の例としては、無機酸化物粒
子から成る層を直接表面上に形成するプラズマ熔射法、
あるいは適当なバインダー中に無機酸化物粒子を分散さ
せて、これを表面上にコーテイングする、ホーローある
いは無機塗装などの方法が挙げられる。In conventional self-cleaning coatings, an "oxidation catalyst" or the like is used to actively oxidize the coating, but the present invention does not rely on that type of reaction. The purification mechanism of the present invention is all about promoting evaporation and vaporization from the object surface. The construction of the surface coating is therefore extremely simple. However, the important point is to suppress active oxidation as much as possible. This point is fundamentally different from conventional self-cleaning coatings. Examples of surface coating in which the method of the present invention is specifically carried out include a plasma spraying method in which a layer of inorganic oxide particles is directly formed on the surface;
Alternatively, methods such as enamel or inorganic coating, in which inorganic oxide particles are dispersed in a suitable binder and coated on the surface, can be used.
これらの中で、実用面での生産性に優れ、しかも比較的
容易に強固な被覆層を得る方法は、無機バインダーを用
いる塗装法が有力な方法として挙げられる。Among these methods, a coating method using an inorganic binder is an effective method for obtaining a strong coating layer with excellent productivity in practical terms and relatively easily.
本発明の実施に好適なバインダーは、金属リン酸塩、ま
たはアルカリ金属ケイ酸塩がある。Binders suitable for the practice of this invention include metal phosphates or alkali metal silicates.
いずれのバインダーの場合にも、有効な組成の構成によ
り、200〜300℃で焼付け硬化を行なうことにより
、極めて強固で安定した金属板上の表面処理が得られる
。通常市販されている、これらのバインダーを用いる塗
料で、500〜600℃の耐熱性と、ホーロー被覆とそ
ん色のない表面物性を示す。本発明に用いる無機酸化物
として必要な性質は、有機物に対1−て積極的な酸化作
用を持たないことが第1の条件である。In the case of any binder, an extremely strong and stable surface treatment on a metal plate can be obtained by carrying out baking hardening at 200 to 300° C. depending on an effective composition. Paints using these binders, which are commonly commercially available, exhibit heat resistance of 500 to 600°C and surface properties that are similar to those of enamel coatings. The first condition required for the inorganic oxide used in the present invention is that it does not have a positive oxidizing effect on organic substances.
金属酸化物のあるものは、酸化触媒として酸化反応を活
性化させる。代表的な酸化触媒として、MnO2.Cu
O,Pt,Pd等が知られているが、この様な化合物は
望ましくない。その理由は灯油の気化面あるいは調理器
庫内表面などで、有機化合物が重炭素質化していく最大
の原因は、空気による酸化、脱水素作用にある。したが
つて、酸化作用のある物質をそこに用いると、この作用
が増幅されて、タール化が逆に促進されてしまうからで
ある。第2の条件は、ある程度の耐熱性を有することで
ある。Some metal oxides activate oxidation reactions as oxidation catalysts. As a typical oxidation catalyst, MnO2. Cu
O, Pt, Pd, etc. are known, but such compounds are undesirable. The reason for this is on the vaporized surface of kerosene or on the inside surface of the cooker, and the biggest cause of organic compounds becoming heavy carbonaceous is oxidation and dehydrogenation in the air. Therefore, if a substance with an oxidizing effect is used there, this effect will be amplified and tar formation will be accelerated. The second condition is that it has a certain degree of heat resistance.
この被覆層を適用する表面の条件からして、温度が加わ
る表面であるため、それ自体が分解したりまたはジッタ
リンクを起こしたりしては、望ましくない。以上の条件
に合致した具体的な化合物としてはM2O3,SlO2
,TiO2,ZnO2,BeOあるいはこれらの複合物
などが挙げられる。Considering the conditions of the surface to which this coating layer is applied, since it is a surface to which temperature is applied, it is undesirable for the coating layer itself to decompose or cause jitter links. Specific compounds that meet the above conditions include M2O3, SlO2
, TiO2, ZnO2, BeO, or a composite thereof.
更に、高温下での適用を考えた場合の望ましい無機酸化
物としては、固体酸としての酸度の大きな化合物は望ま
しくない。Furthermore, compounds with high acidity as solid acids are not desirable as inorganic oxides when considering application under high temperatures.
固体酸としての能力を発揮する場合には、有機物がラジ
カル重合を起こし、重炭素質化する懸念を有するからで
ある。以下に本発明の実施例を中心とした効果を示す。
テストピースとして10−のアルミニウム処理鋼板を用
い、これに表面処理をして、その表面に1μtの大豆油
よりなるサラダ油を100滴点在させて、250℃の炉
中に投じ、30分間の加熱による重量変化から、その浄
化能力の優劣を評価した。一1}、塗料基材として、住
友化学工業の「スミセラム」を用いて、約100μの膜
厚で塗装した。This is because if the organic substance exhibits its ability as a solid acid, there is a concern that the organic substance will undergo radical polymerization and become a heavy carbonaceous substance. Effects of the present invention will be shown below, focusing on examples.
A 10-Aluminium-treated steel plate was used as a test piece, the surface was treated, 100 drops of salad oil made of 1 μt soybean oil was dotted on the surface, and the mixture was placed in a furnace at 250°C and heated for 30 minutes. The purification ability was evaluated based on the weight change. 11}, Sumitomo Chemical's "Sumiceram" was used as the paint base material, and the coating was applied to a film thickness of approximately 100 μm.
「スミセラム」は、リン酸アルミニウムをパインダ一と
して用いた無機塗料である。先ず、プランクの場合、即
ちアルミニウム処理鋼板のみの場合には重量変化率は6
0重量%であつた。次に「スミセラム」のみ塗装した場
合の重量変イ陣&ζ55重量%となり若干減少した。こ
れは塗膜がある程度は凸凹な表面であるため、油の拡散
が悪く、蒸発面積が小さくなつたためかと思われる。次
に、アルミナα−At2O3、およびシリカSiO2)
を添加して、その添加量を5重量%一定としてその無機
酸化物の粒度を変えて、同様の試験をした。試験結果を
次表に示す。表から明らかなように、5〜10μの粒度
の無機化合物が極めて良好である。従来から塗料の添加
物としては、5μ以下の粒度で用いるのが分散性,その
他で通常であるが、その点では、本発明はやや粒子径の
大きなものを用いる訳である。``Sumiceram'' is an inorganic paint that uses aluminum phosphate as a binder. First, in the case of Planck, that is, in the case of only aluminized steel sheets, the weight change rate is 6.
It was 0% by weight. Next, when only "Sumi Ceram" was painted, the weight change was 55% by weight, which was a slight decrease. This is probably because the coating film has a somewhat uneven surface, which causes poor oil diffusion and a small evaporation area. Next, alumina α-At2O3 and silica SiO2)
A similar test was conducted by adding 5% by weight of the inorganic oxide and changing the particle size of the inorganic oxide. The test results are shown in the table below. As is clear from the table, inorganic compounds with a particle size of 5 to 10 microns are very good. Conventionally, additives for paints have been used with a particle size of 5 μm or less for dispersibility and other reasons, but in this respect, the present invention uses particles with a slightly larger particle size.
粒子径が更に大きくなると、塗膜の密着性が明らかに低
下する。テープの引きはがし試験を行なうと、大きな粒
子径の粒子周辺ははがれてしまう。粒径5〜10μの粒
子の添加が良好な理由は、この粒子径の場合、油の表面
上への拡がりが速やかに行なわれ、油の蒸発が有効に進
行するためであると思われる。油の高温下での界面化学
的な性質と、この範囲の粒子径とが、丁度一致するので
はないかと思われる。When the particle size becomes even larger, the adhesion of the coating film clearly decreases. When the tape is peeled off in a test, the area around the large particles peels off. The reason why it is preferable to add particles with a particle size of 5 to 10 μm is thought to be that in the case of this particle size, the oil spreads quickly on the surface and evaporation of the oil proceeds effectively. It seems that the surface chemical properties of oil at high temperatures and the particle size in this range exactly match.
添加する無機酸化物としてアルミナをシリカに代えても
、有効性の差が余りないことから、効果は、上記の様な
物理的な要素に基づくものと考えられる。Even if alumina is replaced with silica as the inorganic oxide to be added, there is not much difference in effectiveness, so it is thought that the effect is based on the above-mentioned physical factors.
次に、粒径5〜10μのアルミナについて、その無機塗
料基材への添加量を変化させて、効果を評価した。Next, the effect of alumina having a particle size of 5 to 10 μm was evaluated by varying the amount added to the inorganic paint base material.
試験結果を図に示す。塗膜物性との関連において、添加
量の上限は40重量%であつた。また添加効果は、約2
重量%の添加量≦ら顕著に現われ、約5〜10重量%の
レベルで飽和する傾向となる。この様な粒径の粒子を含
む状態においては被覆層表面は多孔質となり、滴下した
油の2001)位は残留しているのであるが、表面の光
の反射状態などから、油のシミ跡は全く目立たない状態
であり、とくにそれが顔料を用いて黒色化されていれば
、試験前後の状態差がほとんど分らない。The test results are shown in the figure. In relation to the physical properties of the coating film, the upper limit of the amount added was 40% by weight. The addition effect is approximately 2
This becomes noticeable when the amount added is ≦weight%, and it tends to become saturated at a level of about 5 to 10% by weight. When particles of this size are included, the surface of the coating layer becomes porous, and some of the dropped oil (2001) remains, but oil stains are not visible due to the way the surface reflects light. It is completely inconspicuous, and especially if it has been blackened using pigment, the difference in condition before and after the test is hardly noticeable.
この本発明の方法は、油の滞留によりこれがタール化す
るという問題を含んでいる灯油燃焼バーナなどの気化面
に適用しても、全く同じ様な効果が期待される。The method of the present invention is expected to have exactly the same effect even when applied to vaporizing surfaces such as kerosene combustion burners, which have the problem of oil becoming tar due to stagnation.
このように本発明は方法が単純で、炭素質の堆積が問題
となる各種表面に極めて簡単に適用できて、しかも有効
な炭素質の堆積防止効果が得られるものである。As described above, the method of the present invention is simple and can be applied very easily to various surfaces where carbonaceous deposition is a problem, and moreover, an effective carbonaceous deposition prevention effect can be obtained.
図は無機塗料基材へ添加した粒径5〜10μのアルミナ
の添加量と、被覆層表面上に付着させた油の蒸発,気化
による重量減少率との関係を示す。The figure shows the relationship between the amount of alumina with a particle size of 5 to 10 microns added to the inorganic paint base material and the weight loss rate due to evaporation and vaporization of the oil deposited on the surface of the coating layer.
Claims (1)
アルミナの群から選定した1種以上で粒径が5〜10μ
mのものを2〜40wt%含有する金属リン酸塩あるい
は、アルカリ金属ケイ酸塩から成る被覆層を形成して成
る表面上への炭素質堆積を防止する方法。1. On the surface where you want to prevent carbonaceous deposition, apply one or more selected from the group of silica or alumina with a particle size of 5 to 10μ.
A method for preventing carbonaceous deposition on a surface by forming a coating layer made of a metal phosphate or an alkali metal silicate containing 2 to 40 wt% of m.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14730179A JPS5949314B2 (en) | 1979-11-13 | 1979-11-13 | How to prevent carbonaceous deposits on surfaces |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14730179A JPS5949314B2 (en) | 1979-11-13 | 1979-11-13 | How to prevent carbonaceous deposits on surfaces |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5672174A JPS5672174A (en) | 1981-06-16 |
| JPS5949314B2 true JPS5949314B2 (en) | 1984-12-01 |
Family
ID=15427098
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14730179A Expired JPS5949314B2 (en) | 1979-11-13 | 1979-11-13 | How to prevent carbonaceous deposits on surfaces |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5949314B2 (en) |
-
1979
- 1979-11-13 JP JP14730179A patent/JPS5949314B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5672174A (en) | 1981-06-16 |
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