JPS5922650A - Catalyst unit - Google Patents
Catalyst unitInfo
- Publication number
- JPS5922650A JPS5922650A JP57134547A JP13454782A JPS5922650A JP S5922650 A JPS5922650 A JP S5922650A JP 57134547 A JP57134547 A JP 57134547A JP 13454782 A JP13454782 A JP 13454782A JP S5922650 A JPS5922650 A JP S5922650A
- Authority
- JP
- Japan
- Prior art keywords
- catalyst
- layer
- casing
- temperature
- catalyst layer
- 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
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 70
- 239000003595 mist Substances 0.000 claims abstract description 15
- 239000000779 smoke Substances 0.000 claims description 19
- 229910052751 metal Inorganic materials 0.000 claims description 13
- 239000002184 metal Substances 0.000 claims description 13
- 239000012784 inorganic fiber Substances 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 23
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract description 12
- 239000000377 silicon dioxide Substances 0.000 abstract description 11
- 239000000835 fiber Substances 0.000 abstract description 10
- 229910052697 platinum Inorganic materials 0.000 abstract description 6
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 abstract description 5
- 239000004745 nonwoven fabric Substances 0.000 abstract description 3
- 229910000831 Steel Inorganic materials 0.000 abstract description 2
- 239000002253 acid Substances 0.000 abstract description 2
- 230000004913 activation Effects 0.000 abstract description 2
- 239000010959 steel Substances 0.000 abstract description 2
- 238000011144 upstream manufacturing Methods 0.000 abstract description 2
- 238000003466 welding Methods 0.000 abstract description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- 238000010030 laminating Methods 0.000 abstract 1
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 230000000694 effects Effects 0.000 description 9
- 239000000463 material Substances 0.000 description 7
- 238000010411 cooking Methods 0.000 description 5
- 235000019645 odor Nutrition 0.000 description 5
- 238000001179 sorption measurement Methods 0.000 description 5
- 238000006555 catalytic reaction Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000004744 fabric Substances 0.000 description 4
- 238000009423 ventilation Methods 0.000 description 4
- 238000002485 combustion reaction Methods 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000008157 edible vegetable oil Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 239000011796 hollow space material Substances 0.000 description 2
- 229910000510 noble metal Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- 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
- 238000005273 aeration Methods 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229910000431 copper oxide Inorganic materials 0.000 description 1
- 229910002026 crystalline silica Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 231100000572 poisoning Toxicity 0.000 description 1
- 230000000607 poisoning effect Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 230000000391 smoking effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
Landscapes
- Exhaust Gas Treatment By Means Of Catalyst (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Catalysts (AREA)
- Gas Burners (AREA)
Abstract
Description
【発明の詳細な説明】 産業上の利用分野 この発明は触媒ユニットに関するものである。[Detailed description of the invention] Industrial applications This invention relates to a catalyst unit.
従来例の構成とその問題点
電気ヒータやマイクロ波、さらにガスバーナを用いた調
理用オーブンやレンジ(以下、オーブンを代表させて説
明する)を用いた調理においては、調理に伴う臭気や煙
の発生は避けることができず、昨今の密閉性の高い家屋
釦おいては住環境を悪くすることが多い。このため、通
常は室内の換気を強制的に行なっているが、近時調理器
具の高級化指向によりその設置場所を限定せずに使用す
る傾向があり、換気設備との相対的な距離が広がりつつ
ある。このような現状から、最近では発生源であるオー
ブン自体に、これら臭気や煙を浄化する機能を付与する
試みがなされている。この種の機能を化学的に行わせる
方法としては、触媒反応を利用する方法があり、これま
でにもオーブン庫内壁をホーロ材にし、かつそのホーロ
材そのものに触媒作用を行わしめるべく、金属や金属酸
化物を混入したものが実用に供されている。Conventional configurations and their problems When cooking using electric heaters, microwaves, or gas burner cooking ovens or ranges (hereinafter, ovens will be explained as representative), odors and smoke are generated due to cooking. This is unavoidable, and in today's highly airtight houses, it often makes the living environment worse. For this reason, indoor ventilation is normally forced, but as cooking appliances become more sophisticated these days, there is a tendency to use them without limiting the location where they can be installed, increasing the relative distance between them and the ventilation equipment. It's coming. Under these circumstances, attempts have recently been made to provide the oven itself, which is the source of the odor, with a function to purify these odors and smoke. One way to achieve this type of function chemically is to use a catalytic reaction. Up until now, the inner wall of the oven chamber has been made of hollow material, and in order to make the hollow material itself have a catalytic effect, metal or other materials have been used. Products mixed with metal oxides are in practical use.
一方、オーブンより発生する臭気や煙の原因となる可燃
性成分をオーブン内に取付けた融媒ユニットヲ通して触
媒反応を行わせ燃焼酸化させて除去する方法が提案され
ている。On the other hand, a method has been proposed in which combustible components that cause odor and smoke emitted from the oven are removed by catalytic reaction through a melting medium unit installed in the oven and oxidized by combustion.
微少量の可燃性成分を接触酸化により燃焼除去するため
の触媒としては、貫通孔な有する一体成形触媒や金属網
に触媒を付着させたものなどがある。しかしな力5ら、
これらは比較的低い温度から多量の煙を発生するような
庫内クリーニングヒートサイクル時(庫内壁に付着した
油脂分を除去するための調理目的とは別の空焼き運転)
には有効に煙除去をなしえない。すなわち、多数の貫通
孔を有する一体成形触媒では触媒自体の熱容量が大きく
、排気ガスの潜熱による触媒層の温度上昇は、通過排気
ガス温度よりも大きく時間的遅れが生じ、触媒の反応開
始温度が、庫内の油脂蒸発もしくは分解温度より十分に
低温である場合を除き、触媒層の温度立上シ遅れ期間中
は全くその機能を果さないことになる。また、従来から
用いられているこの種の触媒では、最も効果の高いもの
としては白金を含浸させたものがあるが、この場合でも
動植物油(食用油等)のミスト(蒸気)に対する酸化燃
焼を開始する温度は、油の蒸発温度と同じかあるいはそ
れよりも高いのが普通であり、この点からも、熱容量の
大きい触媒層は好ましいものではない。さらに貫通孔型
の一体成形触媒では油ミストもしくは油煙と触媒壁との
接触を効率的に行わせるためには、流れ方向に接触距離
を大きくとる必要があり、触媒層が大きくならざるを得
ないという欠点がある。Catalysts for burning off minute amounts of combustible components by catalytic oxidation include integrally molded catalysts with through holes and catalysts attached to metal nets. However, power 5 etc.
These are during an internal cleaning heat cycle that generates a large amount of smoke from a relatively low temperature (a dry-burning operation that is not used for cooking purposes to remove fats and oils attached to the internal walls of the refrigerator).
cannot effectively remove smoke. In other words, in the case of an integrally molded catalyst having a large number of through holes, the heat capacity of the catalyst itself is large, and the temperature rise of the catalyst layer due to the latent heat of the exhaust gas has a greater time delay than the temperature of the passing exhaust gas, and the reaction start temperature of the catalyst increases. Unless the temperature is sufficiently lower than the evaporation or decomposition temperature of fats and oils in the refrigerator, the catalyst layer will not perform its function at all during the period of delay in temperature rise of the catalyst layer. In addition, among the conventionally used catalysts of this type, the most effective one is one impregnated with platinum, but even in this case, the oxidative combustion of mist (steam) of animal and vegetable oils (edible oil, etc.) The starting temperature is usually the same as or higher than the evaporation temperature of the oil, and from this point of view as well, a catalyst layer with a large heat capacity is not preferred. Furthermore, in the case of a through-hole type integrally molded catalyst, in order to make efficient contact between the oil mist or oil smoke and the catalyst wall, it is necessary to have a large contact distance in the flow direction, which forces the catalyst layer to be large. There is a drawback.
一方、熱不良を小さくする観点から、金属薄板や網その
ものあるいはその表面に適当触媒を付着させたものは確
かに触媒層そのものの温度の上昇がほぼ排気ガス温度の
上昇に追従しうるが、触媒表面が小さく、多量の油ミス
トや油煙を効果的に処理することは不可能に近いという
欠点がある。On the other hand, from the viewpoint of reducing heat defects, if a suitable catalyst is attached to the thin metal plate or mesh itself or its surface, the temperature rise of the catalyst layer itself can almost follow the rise of the exhaust gas temperature. The disadvantage is that the surface is small and it is almost impossible to effectively treat large amounts of oil mist or smoke.
発明の目的
この発明の目的は、より効率的にオーブンより発生する
油ミストや油煙を除去するための触媒ユニットヲ提供す
ることである。OBJECTS OF THE INVENTION An object of the present invention is to provide a catalyst unit for more efficiently removing oil mist and oil smoke generated from an oven.
発明の構成
この発明の触媒ユニットは、オープン等の庫内または排
気口に取付けられるものであって、排気上流より、金属
メツシュ層と、フィルタ層と、触媒層とをこの順でケー
シング内に積層したものである。Structure of the Invention The catalyst unit of the present invention is installed in an open refrigerator or an exhaust port, and a metal mesh layer, a filter layer, and a catalyst layer are laminated in this order in the casing from the upstream side of the exhaust gas. This is what I did.
ここで、触媒層としては、ンリカ等の無機質繊維の織布
または不織布を担体として用い、この担体に白金などの
貴金属や酸化銅などの金属酸化物を担持したものを用い
ることができる。Here, as the catalyst layer, it is possible to use a woven or nonwoven fabric of inorganic fibers such as phosphoric acid as a carrier, and support a noble metal such as platinum or a metal oxide such as copper oxide on this carrier.
また、前記フィルタ層は前記担体と同様なシリカクロス
もしくはシリカウールからなる一時吸着層である。さら
に、この一時吸着層に接して前段に金属からなる有孔鋼
板。ラス板または網である金属メツシュ層を設け、これ
らを組み合せてケーシング内に収容しユニット化したも
のである。Further, the filter layer is a temporary adsorption layer made of silica cloth or silica wool similar to the carrier. Furthermore, a perforated steel plate made of metal is placed in the preceding stage in contact with this temporary adsorption layer. A metal mesh layer, which is a lath plate or net, is provided, and these are combined and housed in a casing to form a unit.
この発明の触媒ユニットは、熱容量が小さく、かつシリ
カクロスやウールはそれ自体表面積が大きく、特にアル
ミナや結晶シリカをあらかじめ担持させたものでは表面
の熱的安定性も高く、高発熱量を有する油ミストや油煙
の酸化燃焼触媒として効果的である。さらに触媒前段に
設けた一時吸着層であるフィルタ層は比較的分解温度の
高い油ミストを一時この吸着層に付着させておき、排気
ガスの温度上昇t−まって、付着した油ミストを分解し
、ついで触媒層において酸化燃焼させて除去(5)
するという二段階処理を行わせる。さらに、これらの前
段に金属メツシュ層を配設することによって、フィルタ
材や触媒材の機械的な保持のほかに、これらの部材に対
する熱分布の均一化と、排ガス潜熱の熱伝導と全効果的
に行わせることができる。The catalyst unit of this invention has a small heat capacity, and silica cloth and wool themselves have a large surface area, and especially those pre-supported with alumina or crystalline silica have high thermal stability on the surface. Effective as an oxidation combustion catalyst for mist and oil smoke. Furthermore, the filter layer, which is a temporary adsorption layer provided in front of the catalyst, temporarily allows oil mist with a relatively high decomposition temperature to adhere to this adsorption layer, and as the exhaust gas temperature rises, the adhering oil mist is decomposed. Then, a two-step process is carried out in which it is oxidized and burned in the catalyst layer and removed (5). Furthermore, by arranging a metal mesh layer in front of these, in addition to mechanically holding the filter material and catalyst material, it also helps to equalize heat distribution to these components, and improves the heat conduction of exhaust gas latent heat and the overall efficiency. can be made to do so.
実施例の説明
実施例1: 第1図に示すように、シリカファイバを織
って織布とした開孔率40〜70%のシリカクロスの表
面にあらかじめγ−アルミナを5〜15%(重量%、以
下同様)担持させたものに塩化白金酸水溶液を浸漬し、
通常の活性化処理により白金Q、3−wt%を担持した
2枚の触媒層11と、やけシリカファイバの不織布で密
度が0.05〜O,l シ枕のマット(フィルタ層)1
2と、10〜50メツシユのステンレス金鋼(金層メツ
シュ層〕13とを重ね合せ、これらを内径40 far
*外径55□I高さ10圏のアルミメッキ鋼板のケー
シング14に納め、このケーシング14と同、じ内径、
外径の上ぶた151に、ケーシング14に溶接固定して
触媒ユニットヲ得た。Description of Examples Example 1: As shown in Fig. 1, 5 to 15% (wt%) of γ-alumina was preliminarily applied to the surface of a silica cloth with a porosity of 40 to 70%, which was made by weaving silica fibers. , hereinafter the same) immerse the supported material in a chloroplatinic acid aqueous solution,
Two catalyst layers 11 supporting 3-wt% of platinum Q through normal activation treatment, and a mat (filter layer) made of a nonwoven fabric made of burnt silica fibers with a density of 0.05 to O.l
2 and 10 to 50 meshes of stainless steel (gold layer mesh layer) 13, and
*It is housed in a casing 14 made of aluminized steel plate with an outer diameter of 55□I and a height of 10, and has the same inner diameter as this casing 14.
A catalyst unit was obtained by welding and fixing the casing 14 to the outer diameter upper lid 151.
(6)
実施例2: 第2図に示すように、実施例1と同じ触媒
担体に、白金とパラジウムとを重量比で2:10の割合
でかつ総量で担体に対して0.6%を担持して得た触媒
層21と、触媒基材と同じシ゛リカクロスにシリカ−ア
ルミナ(重量比で5:1)20チを担持させた。クロス
状フィルタ層22を2〜3枚重ね合せ、開孔率40〜6
0%の底板〔金属メツシュ層)23t″有する実施例1
とほぼ同寸法のケーシング24内に納め、上ぶた25を
ケーシング24に溶接固定して触媒ユニットを得た。(6) Example 2: As shown in Figure 2, platinum and palladium were added to the same catalyst carrier as in Example 1 at a weight ratio of 2:10 and a total amount of 0.6% based on the carrier. 20 pieces of silica-alumina (5:1 by weight) were supported on the catalyst layer 21 obtained by supporting the catalyst layer 21 and on the same silica cloth as the catalyst base material. Two to three cross-shaped filter layers 22 are stacked, and the porosity is 40 to 6.
Example 1 with 0% bottom plate (metal mesh layer) 23t''
The catalyst unit was housed in a casing 24 having approximately the same dimensions as the catalyst unit, and the upper lid 25 was welded and fixed to the casing 24 to obtain a catalyst unit.
実施例3: 第3図に示すように、あらかじめ波状に成
形した実施例1と同じ触媒層31と、アルミナ・シリカ
繊維を主材料としあらかじめパンチで40〜60チの開
孔率としたセラミック繊維のマット(フィルタ層)32
を重ね合せ、実施例2と同じ開口した底板(金属メツシ
ュ層)33を有するケーシング34内に納め、上ぶた3
5をケーシング34に溶接固定して触媒ユニット全体た
。Example 3: As shown in Fig. 3, the same catalyst layer 31 as in Example 1 was formed into a wave shape in advance, and ceramic fibers made of alumina-silica fibers as the main material and punched in advance to have an aperture of 40 to 60 inches were used. mat (filter layer) 32
are placed in a casing 34 having the same open bottom plate (metal mesh layer) 33 as in Example 2, and the upper lid 3
5 was welded and fixed to the casing 34 to form the entire catalyst unit.
実施例1〜3の触媒ユニットの通気抵抗は、いずれも5
0 !A′ninの通気に対し、10〜60wnH3O
程度であった。The ventilation resistance of the catalyst units of Examples 1 to 3 was 5.
0! 10~60wnH3O for A'nin aeration
It was about.
実施何重ないし3の触媒ユニットを内容積0.1〜0.
2 m3の電気オーブンの排気口に数例け、触媒の効果
をみるために、排気温度検出用としてユニット底部中央
より庫内へ10mm隔てた空間位置と、ユニット内の触
媒の位置とに、それぞれ熱電対を取付け、オーブン内壁
に食用植物性油脂をティースプーンで2〜5杯分塗9つ
けたのち、通電し庫内温度を上昇させた。このときの触
媒層と排気のそれぞれの温度の時間変化は、おおむね第
4図に示すような曲線であった。ここで、排気口からの
発煙は触媒層温度と排気温度が交差するあたりCA点)
から始まり、再びこれらの面温度曲線が接するところ(
B点)で臭気。発煙は完全に停止した。Implement several to three catalyst units with an internal volume of 0.1 to 0.
In order to check the effectiveness of the catalyst, we installed several samples at the exhaust port of a 2 m3 electric oven, one at a space 10 mm away from the center of the bottom of the unit into the oven for exhaust temperature detection, and the other at the location of the catalyst inside the unit. A thermocouple was attached, and after applying 2 to 5 teaspoons of edible vegetable oil to the inner wall of the oven, electricity was turned on to raise the temperature inside the oven. At this time, the temperature changes over time of each of the catalyst layer and the exhaust gas were approximately curved as shown in FIG. 4. Here, smoke is emitted from the exhaust port at point CA, where the catalyst layer temperature and exhaust temperature intersect)
, and again the point where these surface temperature curves touch (
Odor at point B). The smoking stopped completely.
この間の発煙の程度は、排気口近傍よりフィルタ式塵埃
計に排気捕集しフィルタの色調をもって判別した。ここ
で、色調は、着色なし全Oとし、庫内の油脂発火によっ
て発生する煤による着色を5とする6段階法によった。The degree of smoke generated during this period was determined by collecting exhaust gas from the vicinity of the exhaust port using a filter-type dust meter and checking the color tone of the filter. Here, the color tone was determined by a 6-step method in which total O (no coloring) was selected, and coloration due to soot generated by ignition of fats and oils in the refrigerator was set to 5.
また、触媒反応による煙除去効果が明らかに認められる
までの時間を第4図における排気温度の時間依存が、同
一オーブンを使用する限りにおいて、はぼ同じであるこ
とを利用し、ここでは排気温度で示した。In addition, taking advantage of the fact that the time dependence of the exhaust temperature in Figure 4, which takes the time until the smoke removal effect due to the catalytic reaction is clearly recognized, is almost the same as long as the same oven is used, the exhaust temperature It was shown in
比較例: 外径がほぼ同一で、開孔率65%。Comparative example: The outer diameter is almost the same and the porosity is 65%.
高さ10簡のいわゆるモノリス担体に白金を担持した触
媒を比較例として用い、前記と同様にしてフィルタの着
色度および煙減少時の排気温度を測定した。A catalyst in which platinum was supported on a so-called monolithic carrier having a height of 10 pieces was used as a comparative example, and the degree of coloration of the filter and the exhaust gas temperature at the time of smoke reduction were measured in the same manner as described above.
これら実施例1〜3および比較例の試験結果を次表に示
す。The test results of Examples 1 to 3 and Comparative Examples are shown in the following table.
表で明らかなように、比較例に比べていずれの(9)
実施例も消煙効果が高く、シかもオーブン通電後の早い
時期に消煙効果を示している。これは、勲機質繊維の触
媒層を用いたことによりガスと触媒の接触効果が著しく
向上したこと、−!、た触媒層の前段に一時吸着用のフ
ィルタ層を設けたことによシ比較的排気温度の低いとき
に発生する油ミストを直接触媒に付着させずにまずフィ
ルタ層に吸着させ、排気温度の上昇とともに分解脱着し
てより接触反応のしやすいガス体にして触媒と接触させ
たことによる。さらに、触媒表面での反応熱によシ、ユ
ニット全体は排気ガスよシはるかに高い温度と[ハこの
段階においては前段のフィルタ層はほとんど吸着特性を
有しないために、フィルタ層自体の再生クリーニングが
行なわれ、次回の低温度時の油煙発生を阻止する、いわ
ゆる機能回復が自動的に行われることになるのである。As is clear from the table, all of the examples (9) had a higher smoke eliminating effect than the comparative example, and the smoke eliminating effect was exhibited early after the oven was energized. This is due to the fact that the contact effect between the gas and the catalyst has been significantly improved by using the catalyst layer made of organic fibers. By providing a filter layer for temporary adsorption in front of the catalyst layer, oil mist that is generated when the exhaust temperature is relatively low is first adsorbed on the filter layer instead of directly adhering to the catalyst, thereby reducing the exhaust temperature. This is because as it rises, it decomposes and desorbs to form a gas that facilitates catalytic reactions and is brought into contact with the catalyst. Furthermore, due to the heat of reaction on the catalyst surface, the temperature of the entire unit is much higher than that of the exhaust gas. As a result, so-called functional recovery, which prevents the generation of oil smoke at low temperatures the next time, is automatically performed.
さらに、前段の金属メツシュ層による伝熱効果によυ触
媒層の温度上昇速it早め、かつ油ミストの捕集メタル
フィルタとしての効果と、付着した油ミストの分解を早
める効果もある。これらの触媒前段の(10)
フィルタ層および金層メツシ一層の配置は、特に発生す
るものがミストのような液状物であるときに一段とその
効果が著しい。すなわち、触媒表面にこれらミス■・の
付着が生ずると、いわゆる二時被毒的な結果を生み、本
来触媒が気固接触状態で行う場合の反応開始温度では反
応全開始しえないという不具合を解消するものである。Furthermore, the heat transfer effect of the metal mesh layer at the front stage has the effect of accelerating the temperature rise of the υ catalyst layer, and also has the effect of acting as a metal filter for collecting oil mist and accelerating the decomposition of attached oil mist. The arrangement of the (10) filter layer and the gold layer mesh in the front stage of the catalyst is particularly effective when the generated substance is a liquid substance such as mist. In other words, if these mistakes occur on the surface of the catalyst, this results in so-called double poisoning, which causes the problem that the reaction cannot be fully started at the reaction starting temperature when the catalyst is in gas-solid contact. It is something that will be resolved.
なお、前述の実施例においては、無m′R繊維としてシ
リカやシリカ・アルミナ繊維を用いた場合について説明
したが、その他の無槻賀繊維であっても使用可能であり
、たとえばガラス繊維でも特に耐熱性に問題のない場所
に触媒ユニットヲ設置面するならば使用可能である。ま
た、フィルタ層は、必ずしも繊維質繊維を用いたものと
限定されるものでIdなく、その通気抵抗が許されるな
らば(たとえば排気ガスが伺らかの手段で強制排気され
うるものならば)、活性炭やシリカゲルなどでもよい。In the above embodiments, the case where silica or silica-alumina fibers were used as the m'R-free fibers was explained, but other non-m'R fibers can also be used, and for example, glass fibers can also be used. It can be used as long as the catalyst unit is installed in a location where there is no problem with heat resistance. In addition, the filter layer is not necessarily limited to using fibrous fibers, but if its ventilation resistance is allowed (for example, if the exhaust gas can be forcibly exhausted by some means) , activated carbon, silica gel, etc. may also be used.
ただ、これらの場合は当然それらの耐熱性は十分に検討
されねばならない、また触媒物質としては、必ずしも実
施例で用いたような貴金属系に限られる必要はなく、−
わゆるVM属系の金属酸化物であっても排ガス中の成分
を完全酸化するに十分な機能を有するものである。However, in these cases, of course, their heat resistance must be carefully considered, and the catalyst material does not necessarily need to be limited to noble metals as used in the examples.
Even so-called VM metal oxides have a sufficient function to completely oxidize components in exhaust gas.
発明の効果
以上のように、この発明の触媒ユニットは、従来の触媒
ユニットに比してより一層効率的にオーブンやレンジ等
より発生する油ミストや油煙を除去することができると
いう効果がある。Effects of the Invention As described above, the catalyst unit of the present invention has the effect of being able to remove oil mist and oil smoke generated from ovens, ranges, etc. more efficiently than conventional catalyst units.
【図面の簡単な説明】
第1図はこの発明の一実施例を示す断面図、第2図およ
び第3図はこの発明の他の実施例を示す断面図、第4商
は触媒層温度と排気温度との関係を示すグラフである。
11゜21.31・・・触媒層、12.22.32・・
・フィルタ層、13.23.33・・・金属メッンユ層
第1図
第2図
第3図
第4図[Brief Description of the Drawings] Fig. 1 is a sectional view showing one embodiment of the present invention, Figs. 2 and 3 are sectional views showing other embodiments of the invention, and the fourth quotient is the temperature of the catalyst layer. It is a graph showing the relationship with exhaust gas temperature. 11゜21.31...Catalyst layer, 12.22.32...
・Filter layer, 13.23.33...Metal Menyu layer Figure 1 Figure 2 Figure 3 Figure 4
Claims (3)
着するためのフィルタ層と、油ミストや油煙を酸化燃焼
させる触媒層とをこの順で積層した触媒ユニット。(1) A catalyst unit in which a metal mesh layer, a filter layer for temporarily adsorbing oil mist and oil smoke, and a catalyst layer for oxidizing and burning oil mist and oil smoke are laminated in this order.
た特許請求の範囲第(1)項記載の触媒ユニット。(2) The catalyst unit according to claim (1), wherein the catalyst layer supports a catalyst on an inorganic fiber carrier.
相異なる無機質繊維から形成された特許請求の範囲第(
1)項記載の触媒ユニット。(3) The filter layer is formed from an inorganic fiber that is the same as or different from the carrier of the catalyst layer.
Catalyst unit described in section 1).
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57134547A JPS5922650A (en) | 1982-07-30 | 1982-07-30 | Catalyst unit |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP57134547A JPS5922650A (en) | 1982-07-30 | 1982-07-30 | Catalyst unit |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS5922650A true JPS5922650A (en) | 1984-02-04 |
Family
ID=15130863
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP57134547A Pending JPS5922650A (en) | 1982-07-30 | 1982-07-30 | Catalyst unit |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5922650A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0571161A2 (en) * | 1992-05-19 | 1993-11-24 | Prototech Inc. | Filter screen |
US5580535A (en) * | 1994-07-07 | 1996-12-03 | Engelhard Corporation | System and method for abatement of food cooking fumes |
-
1982
- 1982-07-30 JP JP57134547A patent/JPS5922650A/en active Pending
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0571161A2 (en) * | 1992-05-19 | 1993-11-24 | Prototech Inc. | Filter screen |
EP0571161A3 (en) * | 1992-05-19 | 1994-03-23 | Prototech Inc | |
EP0751353A2 (en) * | 1992-05-19 | 1997-01-02 | Prototech Inc. | Filter screen |
EP0751353A3 (en) * | 1992-05-19 | 1997-10-22 | Prototech Inc | Filter screen |
US5580535A (en) * | 1994-07-07 | 1996-12-03 | Engelhard Corporation | System and method for abatement of food cooking fumes |
US5756053A (en) * | 1994-07-07 | 1998-05-26 | Engelhard Corporation | System and method for abatement of food cooking fumes |
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