JPH0360738A - Catalytic body for purification of smoke - Google Patents

Catalytic body for purification of smoke

Info

Publication number
JPH0360738A
JPH0360738A JP19509389A JP19509389A JPH0360738A JP H0360738 A JPH0360738 A JP H0360738A JP 19509389 A JP19509389 A JP 19509389A JP 19509389 A JP19509389 A JP 19509389A JP H0360738 A JPH0360738 A JP H0360738A
Authority
JP
Japan
Prior art keywords
smoke
purification
catalytic body
catalyst
catalysts
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
JP19509389A
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 JP19509389A priority Critical patent/JPH0360738A/en
Publication of JPH0360738A publication Critical patent/JPH0360738A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE:To obtain a low cost catalytic body for purification of smoke having high activity with superior productivity by using CeO2 and a solid basic compd. as oxidation catalysts and mixing them with ceramic fibers and a binder. CONSTITUTION:CeO2 and a solid basic compd. such as SrCO3 or BaCO3 are used as oxidation catalysts. Ceramic fibers of alumina or silica are mixed with a binder and the catalysts are added to the mixture and uniformly mixed. Water is then added so as to attain proper viscosity and the resulting slurry is molded and calcined. A catalytic body for purification of smoke is obtd. at a low cost because a noble metal is not used. This catalytic body is porous, has a high degree of dispersion of the catalysts and high activity and is easily produced.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は石油やガスなどを燃料とする各種燃焼機器やオ
ーブン電子レンジやガステープル等の調理器から排出さ
れる未燃の炭化水素化合物や一酸化炭素を酸化分解する
浄化触媒体に関するものである。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention is directed to the use of unburned hydrocarbon compounds and monoxide discharged from various combustion appliances that use oil, gas, etc. as fuel, and from cooking appliances such as ovens, microwave ovens, and gas stoves. This invention relates to a purification catalyst that oxidizes and decomposes carbon.

従来の技術 例えば調理器を考えた場合、オーブンやグリルでは肉あ
るいは魚等の調理で煙、油煙2臭い等が多量に発生し厨
房が煙で充満したり加熱室内に汚れや臭気が残る等の好
ましくない状況が起こり得る。これを防止するために加
熱室の外に加熱室内の空気を排気孔から強制的に排気す
る排気ファンモータを動作させることにより、食品から
発生する水蒸気・油・煙が加熱室外へ排気され、排気の
途中で浄化触媒体により浄化されるという方式がとられ
ている。浄化触媒体としては白金、パラジウム、I′l
lジウム等の貴金属を、ンリカ、アルミナ等のセラミン
ク粉末粒子を成型、焼成して得られるセラ累ンクハニカ
ム構造体に担持したものが一般的である。また貴金属の
かわりにベロゲスカイト型複合酸化物や、遷移金属の単
独あるいは複合酸化物を担持したものが使用され°ζい
る。
Conventional technology For example, when considering cooking appliances, ovens and grills produce a large amount of smoke, oil smoke, and other odors when cooking meat or fish, and the kitchen is filled with smoke and dirt and odors remain in the heating chamber. Unfavorable situations may arise. To prevent this, by operating an exhaust fan motor that forcibly exhausts the air inside the heating chamber from the exhaust hole outside the heating chamber, water vapor, oil, and smoke generated from the food are exhausted outside the heating chamber. A method is adopted in which the water is purified by a purification catalyst in the middle of the process. As a purification catalyst, platinum, palladium, I'l
Commonly, a noble metal such as l-dium is supported on a ceramic honeycomb structure obtained by molding and firing ceramic powder particles such as phosphoric acid or alumina. In addition, instead of noble metals, vergeskite-type composite oxides and transition metals supported alone or with composite oxides are used.

発明が解法しようとする課題 しかしながら上記したように貴金属を用いるとコストが
非常に高く、またベロゲスカイト型複合酸化物は一般に
は800〜850°C以上という高温で坑底するため表
面積が小さい等の課題がある。
Problems to be Solved by the Invention However, as mentioned above, the cost of using precious metals is extremely high, and the surface area of velogesite-type composite oxides is small because they are generally deposited at the bottom of a mine at a high temperature of 800 to 850°C or higher. There is.

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、酸化触媒としてC
e0zと固体塩基化合物を用い、予めセラミック繊維と
バインダーを混合させてから触媒体を底型し、この触媒
体を用いて調理器の加熱室内の油煙を浄化するものであ
る。
Means for Solving the Problems In order to solve the above problems, the present invention uses C as an oxidation catalyst.
Using e0z and a solid base compound, ceramic fibers and a binder are mixed in advance, a catalyst body is formed into a bottom mold, and this catalyst body is used to purify the oil smoke in the heating chamber of a cooking appliance.

作用 本発明による油煙浄化触媒体の作用について説明する。action The action of the oil smoke purification catalyst body according to the present invention will be explained.

油の構造を(1)式とすると、(R1,R2,R3は飽
和、不飽和のアルキル基)浄化に必要な反応はC−C結
合の切断、二酸化炭素と水への酸化である。
If the structure of oil is represented by formula (1), (R1, R2, and R3 are saturated and unsaturated alkyl groups), the reactions necessary for purification include cutting of C--C bonds and oxidation to carbon dioxide and water.

本浄化触媒体では大気雰囲気下でのCentの酸素供給
と助燃作用と固体塩基による炭素ラジカルの再結合防止
、つまりタール化の抑制という機能を利用して油煙を浄
化するものである。
This purification catalyst purifies oil smoke by utilizing the oxygen supply and auxiliary combustion effect of Cent under atmospheric conditions and the function of preventing carbon radical recombination by solid base, that is, suppressing tar formation.

更に前記したCeOx、固体塩基の混合物をセラミンク
繊維とバインダーを混合した中に予め混入してから底型
し浄化触媒体とするため従来のように後で触媒を担持す
る必要がなく、またセラミック繊維を用いているので気
孔率が高く、触媒の分散度や空気との接触率が高い。
Furthermore, since the aforementioned mixture of CeOx and a solid base is mixed in advance into a mixture of ceramic fibers and a binder and then molded into a bottom mold to form a purification catalyst, there is no need to support the catalyst afterwards as in the conventional case. Since it is used, the porosity is high, and the degree of dispersion of the catalyst and the contact rate with air are high.

実施例 以下本発明の一実施例を図面を用いて説明する。Example An embodiment of the present invention will be described below with reference to the drawings.

まず製造方法について説明する。First, the manufacturing method will be explained.

Centは硝酸セリウム水溶液にアンモニア水を加えて
水和物の形で共沈させ、十分に水洗してアルカリの徐々
を行った後、乾燥、坑底して得られた比表面積の大きい
(約180nf/g)ものを用い、固体塩基として市販
の試薬の5rCO,を用いた。
Cent is a product with a large specific surface area (approximately 180nf) that is obtained by adding ammonia water to an aqueous cerium nitrate solution, co-precipitating it in the form of a hydrate, thoroughly washing it with water to gradually remove the alkali, and drying it at the bottom of the mine. /g), and a commercially available reagent 5rCO was used as the solid base.

まずCeOxとS r C03をモル比で1=1の割合
で秤量し2時間自動混練機で混練した。
First, CeOx and S r C03 were weighed in a molar ratio of 1=1 and kneaded for 2 hours using an automatic kneader.

次にアル柔す・シリカ系セラミック繊維6帽1%、Zn
O−B2us’ S fox系ガラス粉末10重量%、
前記したC e Ox 、 S r COxの混合物3
0重量%を均一に混合した後、適当な粘度になるように
水を加えてスラリーを作成した。次に前記したスラリー
を抄紙法により厚さ約0.5mのセラくツクシートを形
成し、その後大気中600’Cで1時間焼成した。更に
コルゲータ−にまり片段加工した後、戒巻もしくは積層
させてハニカム状に成形加工した。
Next, Al-softened silica-based ceramic fiber 6 caps 1%, Zn
O-B2us'S fox glass powder 10% by weight,
Mixture 3 of C e Ox and S r COx described above
After uniformly mixing 0% by weight, water was added to obtain a suitable viscosity to prepare a slurry. Next, a ceramic sheet having a thickness of about 0.5 m was formed using the above-mentioned slurry by a papermaking method, and then fired in the air at 600'C for 1 hour. Furthermore, after being processed in one stage by corrugator, it was formed into a honeycomb shape by being wrapped or laminated.

次にCeO,、固体塩基の特性について具体的に説明す
る。
Next, the characteristics of CeO, a solid base, will be specifically explained.

まずCe0zは、粉末状態で表面積が広く、また多量の
酸素を吸蔵することができるため助触媒どしての用途も
多い。またCeの陽イオンは3価と4価の間の酸化還元
が容易なので液相酸化の触媒となることが知られている
First, Ce0z has a large surface area in powder form and can store a large amount of oxygen, so it is often used as a cocatalyst. Furthermore, it is known that Ce cations can easily undergo redox between trivalent and tetravalent ions, and thus serve as a catalyst for liquid phase oxidation.

実際にCe0rの粉末上にサラダ油を滴下して加熱する
と、200°C位から煙を上げて燃え始めた。
When salad oil was actually dropped onto Ce0r powder and heated, it began to burn and emit smoke at around 200°C.

第1図■にCe Oz粉末20■にサラダ油5μlを滴
下し熱天秤を用いて昇温によるサラダ油の重量変化特性
を測定した結果を示す。
Figure 1 (2) shows the results of dropping 5 μl of salad oil onto 20 cm of CeOz powder and measuring the weight change characteristics of the salad oil due to temperature rise using a thermobalance.

しかしサラダ油等の炭化水素は分解と同時に再結合によ
り環状結合、不飽和結合が生成し、触媒表面に化学吸着
し浄化されずにタール化して残る。
However, when hydrocarbons such as salad oil are decomposed and recombined, cyclic bonds and unsaturated bonds are generated, which are chemically adsorbed onto the catalyst surface and remain as tar without being purified.

この現象は第1図ので300’Cから徐々に500°C
まで温度を上げてもサラダ油は完全に焼き切れ・ず徐々
に重量が減少し続けることから実証される。そこで5r
COx等の固体塩基を添加して生成した炭素ラジカルと
塩基を反発させ、炭素ラジカルの触媒表面への吸着を防
止し、炭素ラジカルの安定化をはかりタール化を抑制す
る。
As shown in Figure 1, this phenomenon gradually increases from 300'C to 500'C.
This is proven by the fact that even if the temperature is raised to 1, the salad oil is not completely burnt out and its weight continues to gradually decrease. So 5r
A solid base such as COx is added to repel generated carbon radicals and the base, thereby preventing adsorption of carbon radicals to the catalyst surface, stabilizing carbon radicals, and suppressing tar formation.

第1図■にS r COs粉末20■にサラダ油5μl
を滴下し、上記したC e Oxの場合と同じ条件で熱
天秤を用いて昇温によるサラダ油の重量変化特性を測定
した結果を示す。
Figure 1 ■: Sr COs powder: 20■: salad oil: 5 μl
The results are shown in which the weight change characteristics of salad oil due to temperature rise were measured using a thermobalance under the same conditions as in the case of C e Ox described above.

S r COsでは350°Cまでは油の重量減少は少
ないが、350’Cを越えると重量が急激に減少して油
が焼き切れるのが特徴的である。
In S r COs, the weight loss of oil is small up to 350°C, but when the temperature exceeds 350'C, the weight suddenly decreases and the oil is burnt out.

ホットプレート上で5rCO,I粉末にサラダ油を溝下
して加熱した場合にも油は徐々に黒くタール化し、35
0°Cを越えると表面からサーフと黒色物質が消失する
のが観察された。
Even when salad oil was added to 5rCO,I powder on a hot plate and heated, the oil gradually turned black and turned into tar.
Surf and black material were observed to disappear from the surface above 0°C.

本発明の油煙浄化触媒体は、比表面積が大きく助燃作用
の強いCeO,とタール化を抑制する固体塩基化合物の
混合物を、空隙率の高いセラミンク繊維多孔体中に分散
させて底型しである。そこで調理物から出たミスト状の
油分や未燃ガスを含む排ガス気流中に配置され、完全酸
化に必要な温度まで加熱されると、前記触媒体を通過す
る排ガス中の未燃の炭化水素、−酸化炭素は触媒体上で
酸素と共に触媒し酸化反応により二酸化炭素と水蒸気に
変換されるのである。
The oil smoke purification catalyst of the present invention has a bottom type in which a mixture of CeO, which has a large specific surface area and has a strong combustion-supporting effect, and a solid base compound that suppresses tar formation is dispersed in a ceramic fiber porous body with a high porosity. . There, the catalyst body is placed in an exhaust gas stream containing mist-like oil and unburned gas from the cooked food, and when heated to the temperature required for complete oxidation, the unburned hydrocarbons in the exhaust gas that pass through the catalyst body, - Carbon oxide is catalyzed together with oxygen on the catalyst body and converted into carbon dioxide and water vapor through an oxidation reaction.

発明の効果 以上のように本発明の浄化触媒体は、触媒として酸化物
と炭酸塩の混合物を用いているため触媒調製(焼成も含
む)が非常に簡単であり、またあらかじめ酸化触媒とセ
ラミック繊維とバインダーを混合させその後成型するた
め従来のように後で触媒を担持する必要がない。
Effects of the Invention As described above, the purification catalyst of the present invention uses a mixture of oxide and carbonate as a catalyst, so catalyst preparation (including calcination) is very simple. Since it is mixed with a binder and then molded, there is no need to support a catalyst afterwards as in the conventional method.

従って生産性に優れており低コストである。またセラ【
ツク繊維を用いているので多孔質であり、触媒の分散度
が高く活性点も多くなるため高活性化が実現される。
Therefore, productivity is excellent and cost is low. Also Sera [
Because it uses tsuku fiber, it is porous, and the catalyst has a high degree of dispersion and a large number of active sites, achieving high activation.

またCeO,と固定塩基の化合物であるため白〜淡黄色
の触媒体であり任意な色への着色も可能である。更にC
eO,は加熱されると黄変し、温度が下がると元に戻る
サーモクロミズム特性を持っているため触媒体の温度上
昇が視覚的にわかるという特徴を持っている。
Furthermore, since it is a compound of CeO and a fixed base, it is a white to pale yellow catalyst and can be colored in any color. Further C
eO, has a thermochromic property that turns yellow when heated and returns to its original state when the temperature drops, so it has the characteristic that the rise in temperature of the catalyst can be visually detected.

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

図は本発明の一実施例における油煙浄化触媒体のCeO
,と5rCOsの熱天秤によるTGカーブを示した特性
図である。
The figure shows CeO of an oil smoke purification catalyst in one embodiment of the present invention.
, and 5rCOs using a thermobalance.

Claims (3)

【特許請求の範囲】[Claims] (1)セラミック繊維とバインダーと、酸化触媒である
CeO_2及び固体塩基化合物とよりなる油煙浄化触媒
体。
(1) An oil smoke purification catalyst body consisting of ceramic fibers, a binder, CeO_2 as an oxidation catalyst, and a solid base compound.
(2)セラミック繊維がシリカ、アルミナのうちの少な
くとも、1種からなる特許請求の範囲第(1)項記載の
油煙浄化触媒体。
(2) The oil smoke purification catalyst according to claim (1), wherein the ceramic fibers are made of at least one of silica and alumina.
(3)固体塩基化合物がSrCO_3、BaCO_3、
のいずれか1つである特許請求の範囲第(1)項記載の
油煙浄化触媒体。
(3) The solid base compound is SrCO_3, BaCO_3,
The oil smoke purification catalyst body according to claim (1), which is any one of the following.
JP19509389A 1989-07-26 1989-07-26 Catalytic body for purification of smoke Pending JPH0360738A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19509389A JPH0360738A (en) 1989-07-26 1989-07-26 Catalytic body for purification of smoke

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19509389A JPH0360738A (en) 1989-07-26 1989-07-26 Catalytic body for purification of smoke

Publications (1)

Publication Number Publication Date
JPH0360738A true JPH0360738A (en) 1991-03-15

Family

ID=16335417

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19509389A Pending JPH0360738A (en) 1989-07-26 1989-07-26 Catalytic body for purification of smoke

Country Status (1)

Country Link
JP (1) JPH0360738A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6790807B2 (en) 2001-09-13 2004-09-14 Rothmans, Benson & Hedges Inc. Zirconium/metal oxide fibers

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6790807B2 (en) 2001-09-13 2004-09-14 Rothmans, Benson & Hedges Inc. Zirconium/metal oxide fibers

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