JPS61147014A - Catalytic burner - Google Patents

Catalytic burner

Info

Publication number
JPS61147014A
JPS61147014A JP59269932A JP26993284A JPS61147014A JP S61147014 A JPS61147014 A JP S61147014A JP 59269932 A JP59269932 A JP 59269932A JP 26993284 A JP26993284 A JP 26993284A JP S61147014 A JPS61147014 A JP S61147014A
Authority
JP
Japan
Prior art keywords
combustion
layer
catalyst layer
combustion catalyst
fuel gas
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.)
Granted
Application number
JP59269932A
Other languages
Japanese (ja)
Other versions
JPH0335574B2 (en
Inventor
Ryoji Shimada
良治 島田
Yoshiyuki Gokajiya
後梶谷 嘉之
Ikuo Matsumoto
松本 郁夫
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 JP59269932A priority Critical patent/JPS61147014A/en
Publication of JPS61147014A publication Critical patent/JPS61147014A/en
Publication of JPH0335574B2 publication Critical patent/JPH0335574B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23DBURNERS
    • F23D14/00Burners for combustion of a gas, e.g. of a gas stored under pressure as a liquid
    • F23D14/12Radiant burners
    • F23D14/18Radiant burners using catalysis for flameless combustion

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Combustion & Propulsion (AREA)
  • Mechanical Engineering (AREA)
  • General Engineering & Computer Science (AREA)
  • Gas Burners (AREA)

Abstract

PURPOSE:To promote an effective oxidative reaction and reduce amount of catalysts by a method wherein a catalytic body for combustion purpose containing an oxidative catalyst in a ceramic body are divided into three layers, among them, the rear surface layer faced to a fuel supplying unit, and the other of the front surface accessed to a diffusing air, are formed with a lower rate of carrying capacities compared with the middle layer. CONSTITUTION:When a thermo-couple 12 to detect a combustion temperature detects a preheating temperature exceeding a given level an electric-magnetic valve is energized to open valve, thereby fuel is supplied. The supplied fuel gas is filled in a gas chamber 4 with a full, which is diffusing uniformly inside of a thermal insulation diffusing member 5 to reach the rear surface of combustion layer 7, where combustion gas is partly oxidized to generate a heat, thereby the both temperatures of rear surface combustion of catalyst layer 7 and the middle combustion catalyst lever 8 are increased. The fuel gas passing through the rear surface combustion catalysts layer 7, during which a partial oxidative reaction is being generated, proceeded to the middle combustion catalyst layer 8, where oxidative reaction is rapidly promoted by a combustion air internally being diffused, simultaneously the temperature of the middle combustion catalyst layer 8 is rapidly increased up to 500 deg.C. When the fuel gas, which is mostly oxidized more than half so far, has reached the front surface combustion catalyst layer 9, the fuel gas has been completely oxidized there.

Description

【発明の詳細な説明】 産業上の利用分野 本発明は、触媒体上に気体燃料あるいは気化させた液体
燃料を供給し、燃焼用空気によって前記の燃料を触媒酸
化させ、その反応により生じた燃焼熱および輻射熱を利
用する触媒バーナに関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention supplies gaseous fuel or vaporized liquid fuel onto a catalyst body, catalytically oxidizes the fuel with combustion air, and oxidizes the combustion produced by the reaction. This invention relates to a catalytic burner that utilizes heat and radiant heat.

従来の技術 従来この種の触媒バーナけ、第2図に示すように多数の
小孔を有した燃料分散管11に裏面から設置したバーナ
ケース2内に、拡散材3とPt、Rh。
BACKGROUND OF THE INVENTION Conventionally, as shown in FIG. 2, in this type of catalyst burner, a diffusion material 3, Pt, and Rh are placed in a burner case 2, which is installed from the back side into a fuel dispersion pipe 11 having a large number of small holes.

P(i等の白金族金属の内1種類以上を用いた酸化触媒
を一定の担持率で担持した単一の燃焼用触媒層4を設け
た構成になっ℃おり、燃料分散管1から送入されたガス
燃料は拡散材3の内部を均一に拡散しながら燃焼用触媒
層4内に至り、何らかの着火手段で着火された後、燃焼
用触媒層40表面上で定常的な触媒燃焼が行われるよう
になっていた。(例えば、特開昭58−213110号
公報)発明が解決しようとする問題点 しかしながら上記構成では、燃焼用触媒層4の大気側、
中央部、裏面部でそれぞれ反応性が異なるため各部の温
度も違いが生じる。特に燃焼用触媒層の裏面部付近は燃
料ガスの燃焼用空気に対する割合が非常に大であるため
、燃料ガスの一部しか反応しないのに対し、燃焼用触媒
層の中央部に燃料ガスが至れば、燃焼用空気の存在する
割合が大きくなり、反応は急激に進行するため急激に反
応温度は上昇する。また燃焼用触媒層4の大気側に近い
部分に燃料ガスが至る頃には、中央部で反応しきれなか
った残余の燃料ガスが大量の拡散空気によって酸化され
るため生じる反応熱は大ではなく、同時に生じた反応熱
を放出し、また拡散空気の冷却作用も影響するため、最
も低温部分を形成する。したがって、定常触媒酸化反応
中の燃焼用触媒層4の温度分布は、中央部が最も高温で
、次いで裏面付近、大気側付近となる。したがって理想
的な酸化触媒の担持率の分布も中央部が最も多量に必要
とし1反応に関与する割合の低い裏面部では低担持率で
すみ、また燃焼用空気が大量に存在する大気側付近は中
央部よりも低担持率′ですむ。しかるに酸化触媒の担持
率が各部で一定の単一の燃焼用触媒層4では、反応性に
対応した担持率分布とナリ得す、特に酸化触媒に白金族
金属等の高価なものを用いた場合、燃焼に必要な量の酸
化触媒量を得るためには相当な高コストを覚悟しなけれ
ばならなかった。
The composition includes a single combustion catalyst layer 4 that supports an oxidation catalyst using one or more platinum group metals such as P(i) at a constant loading rate, and the fuel is fed from the fuel dispersion pipe 1. The gas fuel reaches the combustion catalyst layer 4 while uniformly diffusing inside the diffusion material 3, and after being ignited by some kind of ignition means, steady catalytic combustion is performed on the surface of the combustion catalyst layer 40. (For example, Japanese Unexamined Patent Publication No. 58-213110) Problems to be Solved by the Invention However, in the above structure, the atmosphere side of the combustion catalyst layer 4,
Since the reactivity differs between the center and the back surface, the temperature of each region also differs. In particular, near the back surface of the combustion catalyst layer, the ratio of fuel gas to combustion air is very large, so only a portion of the fuel gas reacts, whereas the fuel gas reaches the center of the combustion catalyst layer. For example, the proportion of combustion air present increases, and the reaction proceeds rapidly, resulting in a rapid rise in reaction temperature. Furthermore, by the time the fuel gas reaches the part of the combustion catalyst layer 4 close to the atmosphere, the residual fuel gas that has not completely reacted in the central part is oxidized by a large amount of diffused air, so the reaction heat generated is not large. At the same time, the generated reaction heat is released, and the cooling effect of the diffused air also affects the temperature, so it forms the coldest part. Therefore, the temperature distribution of the combustion catalyst layer 4 during the steady catalytic oxidation reaction has the highest temperature at the center, followed by the back surface and the atmosphere side. Therefore, the ideal distribution of the oxidation catalyst loading rate is such that the central part requires the most amount, while the back side, where the proportion involved in one reaction is low, has a low loading rate. The loading rate is lower than that in the center. However, in a single combustion catalyst layer 4 in which the oxidation catalyst loading rate is constant in each part, a loading rate distribution that corresponds to the reactivity can be obtained, especially when an expensive oxidation catalyst such as a platinum group metal is used. However, in order to obtain the amount of oxidation catalyst necessary for combustion, it was necessary to prepare for a considerably high cost.

本発明はかかる従来の問題点を解消するもので、燃焼用
触媒体の各層を反応性に応じた触媒性能とし、効率的な
酸化反応をさせ、かつ全体的な触媒量の節減を行うこと
を目的とする。
The present invention solves these conventional problems by making each layer of the combustion catalyst have catalytic performance according to its reactivity, allowing efficient oxidation reaction, and reducing the overall amount of catalyst. purpose.

問題点を解決するための手段 上記の問題点を解決するために、本発明の触媒バーナは
、耐熱性セラミ・ツク担体に酸化触媒を担持した燃焼用
触媒体を3層に分け、燃料供給部に近い裏面層と拡散空
気に近接する表面層の部分を中央層よりも低い担持率に
したものである。
Means for Solving the Problems In order to solve the above problems, the catalytic burner of the present invention has a combustion catalyst body in which an oxidation catalyst is supported on a heat-resistant ceramic carrier divided into three layers, and a fuel supply section. The back layer close to the central layer and the surface layer close to the diffusion air have lower loading rates than the central layer.

作用 本発明は上記の構成によって、燃料供給部から供給され
た燃料ガスが燃焼用触媒体の裏面層で一部反応し、温度
上昇しながら最も酸化触媒の担持率の高い中央層に至り
、急激に反応が進み、同時に急激に温度上昇しながら表
面層に至る。表面層では、燃料ガスの大半が燃焼し、未
燃成分の完全燃焼の段階となる。したがって中央層にお
ける酸化触媒の担持率を裏面層、表面層よりも比較的多
くして効率のよい、安価なものとなる。
According to the above-described structure, the fuel gas supplied from the fuel supply section partially reacts on the back layer of the combustion catalyst body, and reaches the center layer where the oxidation catalyst is supported the highest while increasing the temperature, and rapidly The reaction progresses, and at the same time the temperature rises rapidly and reaches the surface layer. In the surface layer, most of the fuel gas is combusted, and unburned components are completely combusted. Therefore, the supporting ratio of the oxidation catalyst in the center layer is relatively higher than that in the back layer and the surface layer, resulting in an efficient and inexpensive product.

実施例 以下、本発明の一実施例を添付の図面に基いて説明を行
う。
EXAMPLE Hereinafter, an example of the present invention will be explained based on the accompanying drawings.

第1図に於て、耐熱性金属からなるバーナケース1の下
部には燃料分散ノズル2が貫通設置され。
In FIG. 1, a fuel dispersion nozzle 2 is installed through the lower part of a burner case 1 made of a heat-resistant metal.

通気抵抗が無視できる程度の高い開孔度を有する金網め
るいはラス網形式のスペーサ3と前記バーナケース1に
よりガス室4が形成されている。一方、スペーサ3から
前方には、スペーサ3に近接した部分から耐熱性セラミ
ック繊維成型体からなる保温拡散材6、ニクロムヒータ
線を一定パターンで分布させた予熱器6、ムe203・
5io2等の微小細孔を有しかつ高い比表面積を有する
耐熱性セラミ・アク繊維成型体を担体とし、0.2〜0
.3%のRhの担持率を有する裏面燃焼用触媒層7、同
様の担体に0.5〜1俤のRh担持率を有する中央燃焼
用触媒118、さらに同様の担体に0.2〜0.3チの
Rh担持率を有する表面燃焼用触媒1i9があり、表面
燃焼用触媒層9の前面は通気抵抗をほとんど無視できる
程度の高い開孔度を有する金網あるいはラス網からなる
保護ネット1oによって保持されており、保護ネット1
0はその外周部を保持金具11によって固定されている
。また、裏面燃焼用触媒1ii7と中央燃焼用触媒層8
0間には燃焼温度検知用の熱電対12が設置されている
A gas chamber 4 is formed by the burner case 1 and a spacer 3 in the form of a wire mesh or lath mesh having a high degree of aperture so that ventilation resistance is negligible. On the other hand, in front of the spacer 3, in the vicinity of the spacer 3, there is a heat insulating diffusion material 6 made of a heat-resistant ceramic fiber molded body, a preheater 6 in which nichrome heater wires are distributed in a fixed pattern, and a mu e203.
A heat-resistant ceramic/ac fiber molded body having micropores such as 5io2 and a high specific surface area is used as a carrier, and 0.2 to 0
.. A back combustion catalyst layer 7 having a Rh loading rate of 3%, a central combustion catalyst 118 having a Rh loading rate of 0.5 to 1 ton on a similar carrier, and a further 0.2 to 0.3 ton on a similar carrier. There is a surface combustion catalyst 1i9 having a Rh loading ratio of Protective net 1
0 is fixed at its outer periphery by a holding fitting 11. In addition, the back combustion catalyst 1ii7 and the central combustion catalyst layer 8
A thermocouple 12 for combustion temperature detection is installed between the two.

次に上記構成に於ける作用を説明する。Next, the operation of the above configuration will be explained.

予熱器6に通電されると、発生した熱は裏面燃焼用触媒
1ij7から表面燃焼用触媒層9へ伝達され、裏面燃焼
用触媒層7と中央燃焼用触媒層8の間の温度が一定の温
度(260〜300’C)に到達するまで通電が続行さ
れる。そして、燃焼温度検知用の熱電対12が一定温度
以上に予熱が進んだことを感知すると、燃料ガス供給用
の電磁弁(図示せず)にも通電され、燃料が供給される
。供給芒れた燃料ガスは燃料分散ノズル2によってガス
室4内に充満し、保温拡散材6内を均一に拡散しながら
、裏面燃焼用触媒層7に至り燃料ガスの一部が酸化され
、発生した熱によって裏面燃焼用触媒層7、中央燃焼用
触媒Iw8の温度が上昇する。一部反応しながら裏面燃
焼用触媒層7を通過した燃料ガスは中央燃焼用触媒層8
に至って、内部に拡散してくる燃焼用空気により急激に
酸化され、同時に中央燃焼用触媒層9の温度も500°
C程度に急上昇する。さらに大半が酸化された燃料ガス
は表面燃焼用触媒+99に至ってほぼ完全に酸化される
。この段階では予熱器6は必要とせず、予熱器6への通
電は停止される。
When the preheater 6 is energized, the generated heat is transferred from the back combustion catalyst 1ij7 to the front combustion catalyst layer 9, and the temperature between the back combustion catalyst layer 7 and the center combustion catalyst layer 8 is kept constant. The energization is continued until the temperature reaches (260 to 300'C). When the thermocouple 12 for detecting combustion temperature detects that preheating has progressed to a certain temperature or higher, a solenoid valve (not shown) for supplying fuel gas is also energized, and fuel is supplied. The supplied fuel gas fills the gas chamber 4 through the fuel dispersion nozzle 2, and while uniformly diffusing inside the heat-insulating diffusion material 6, reaches the back combustion catalyst layer 7, where a part of the fuel gas is oxidized and generated. The heat causes the temperatures of the back combustion catalyst layer 7 and the central combustion catalyst Iw8 to rise. The fuel gas that has passed through the back side combustion catalyst layer 7 while partially reacting is transferred to the center combustion catalyst layer 8.
At this point, it is rapidly oxidized by the combustion air that diffuses inside, and at the same time, the temperature of the central combustion catalyst layer 9 also increases to 500°.
It rises rapidly to about C. Further, the fuel gas, most of which has been oxidized, reaches the surface combustion catalyst +99 and is almost completely oxidized. At this stage, the preheater 6 is not required, and the power supply to the preheater 6 is stopped.

この時、表面燃焼用触媒19は中央燃焼用触媒層での燃
焼熱の伝熱と、自己の反応熱を得るが、それにも増して
輻射熱としての熱放出、拡散空気の冷却作用が強いため
、表面燃焼用触媒層9の温度は最も低く260〜350
’C程度となる。このようにして裏面燃焼用触媒層7.
中央燃焼用触媒層80表面燃焼用触媒層9の各層での触
媒燃焼は定常状態に至る。中央燃焼用触媒層8のRh担
持率は、他の2層に比べ高くなっているが、担体として
、1oO〜200d/9といった高い比表面積を有し、
800〜900°Cといった高い耐熱性を有するムe2
05・Sio2を用いているため、460〜550’C
の燃焼温度を保持している中央燃焼用触媒層8でも、触
媒粒子は比較的高分散で微粒子状態を保持できる。また
、表面燃焼用触媒層9の酸化触媒の担持率は中央燃焼用
触媒層8の酸化触媒の担持率よりも低いため、表面燃焼
用触媒層9の酸化触媒粒子の分散度は中央燃焼用触媒層
8における分散度よりも高く、極めて良好な微粒子状態
を保持できる。さらに、表面燃焼用触媒層9での反応温
度が250〜350°C程度であることからシンタリン
グの心配は全くない。
At this time, the surface combustion catalyst 19 transfers the combustion heat in the central combustion catalyst layer and obtains its own reaction heat, but it also releases heat as radiant heat and has a strong cooling effect of the diffused air. The temperature of the surface combustion catalyst layer 9 is the lowest, 260 to 350.
It will be about C. In this way, the back side combustion catalyst layer 7.
Catalytic combustion in each layer of the central combustion catalyst layer 80 and the surface combustion catalyst layer 9 reaches a steady state. The Rh loading rate of the central combustion catalyst layer 8 is higher than that of the other two layers, but as a carrier, it has a high specific surface area of 100 to 200 d/9,
Mu e2 with high heat resistance of 800-900°C
05・Sio2 is used, so the temperature is 460~550'C
Even in the central combustion catalyst layer 8 which maintains a combustion temperature of , the catalyst particles are relatively highly dispersed and can maintain a fine particle state. Furthermore, since the supporting rate of the oxidation catalyst in the surface combustion catalyst layer 9 is lower than the supporting rate of the oxidation catalyst in the central combustion catalyst layer 8, the degree of dispersion of the oxidation catalyst particles in the surface combustion catalyst layer 9 is lower than that of the central combustion catalyst layer. The degree of dispersion is higher than that in layer 8, and an extremely good state of fine particles can be maintained. Furthermore, since the reaction temperature in the surface combustion catalyst layer 9 is about 250 to 350°C, there is no fear of sintering.

発明の効果 以上のように本発明の触媒バーナによれば、以下のよう
な効果が得られる。
Effects of the Invention As described above, the catalytic burner of the present invention provides the following effects.

(1)燃焼用触媒体を3層に分割し、表面層と裏面層の
酸化触媒の担持率を中央層の酸化触媒の担持率よりも少
くしたことにより、中央層での反応性よりも低い反応性
を有する表面層と裏面層に於ける酸化触媒の童を節減す
ることができる。
(1) The combustion catalyst body is divided into three layers, and the oxidation catalyst loading rate on the front and back layers is lower than the oxidation catalyst loading rate in the middle layer, resulting in lower reactivity than in the middle layer. The amount of oxidation catalyst in the reactive surface layer and back layer can be reduced.

(2)  上記構成により、一定の担持率に固定した単
一の燃焼用触媒体の場合よりも、触媒金属の所要量を節
減することができる。
(2) With the above configuration, the required amount of catalyst metal can be reduced compared to the case of a single combustion catalyst body with a fixed loading rate.

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

第1図は本発明の一実施例である触媒バーナの縦断面図
、第2図は従来の触媒バーナの縦断面図である。 2・・・・・・燃料分散ノズル、7・・・・・・裏面燃
焼用触媒層、8・・・・・・中央燃焼用触媒層、9・・
・・・・表面燃焼用触媒層。 代理人の氏名 弁理士 中 尾 敏 男 ほか1名菓 
1 図
FIG. 1 is a longitudinal sectional view of a catalytic burner according to an embodiment of the present invention, and FIG. 2 is a longitudinal sectional view of a conventional catalytic burner. 2... Fuel dispersion nozzle, 7... Back combustion catalyst layer, 8... Central combustion catalyst layer, 9...
...Catalyst layer for surface combustion. Name of agent: Patent attorney Toshio Nakao and one other name
1 figure

Claims (3)

【特許請求の範囲】[Claims] (1)セラミック繊維からなる非圧縮成型体、あるいは
織布、又は多孔体等の内1種類を担体とし、酸化触媒を
担持した燃焼用触媒体を3層に分割し燃料供給部に近い
層および外気に面した層の酸化触媒の担持率をこの2つ
の層の間に位置する中央の層の酸化触媒の担持率よりも
少くした触媒バーナ。
(1) Using one type of carrier such as a non-compression molded body made of ceramic fibers, a woven fabric, or a porous body, the combustion catalyst body carrying an oxidation catalyst is divided into three layers, and the layer near the fuel supply part and the A catalytic burner in which the oxidation catalyst loading rate in the layer facing the outside air is lower than the oxidation catalyst loading rate in the central layer located between these two layers.
(2)燃焼用触媒体の担体としてγ−Al_2O_3、
Al_2O_3・SiO_2、SiO_2等の多孔質か
つ高い比表面積を有するセラミックスを用いた特許請求
の範囲第1項記載の触媒バーナ。
(2) γ-Al_2O_3 as a carrier for the combustion catalyst;
The catalytic burner according to claim 1, which uses ceramics that are porous and have a high specific surface area, such as Al_2O_3.SiO_2 and SiO_2.
(3)酸化触媒として、Pt、Pd、Rh等の白金族金
属の内1種類以上、またはLa、Co、Ce、Sr等か
らなるペロブスカイト型構造を有する酸化物等を用いた
特許請求の範囲第1項記載の触媒バーナ。
(3) As an oxidation catalyst, one or more of platinum group metals such as Pt, Pd, Rh, etc., or an oxide having a perovskite structure consisting of La, Co, Ce, Sr, etc. is used as the oxidation catalyst. Catalytic burner according to item 1.
JP59269932A 1984-12-21 1984-12-21 Catalytic burner Granted JPS61147014A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59269932A JPS61147014A (en) 1984-12-21 1984-12-21 Catalytic burner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59269932A JPS61147014A (en) 1984-12-21 1984-12-21 Catalytic burner

Publications (2)

Publication Number Publication Date
JPS61147014A true JPS61147014A (en) 1986-07-04
JPH0335574B2 JPH0335574B2 (en) 1991-05-28

Family

ID=17479203

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59269932A Granted JPS61147014A (en) 1984-12-21 1984-12-21 Catalytic burner

Country Status (1)

Country Link
JP (1) JPS61147014A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5248251A (en) * 1990-11-26 1993-09-28 Catalytica, Inc. Graded palladium-containing partial combustion catalyst and a process for using it
US5250489A (en) * 1990-11-26 1993-10-05 Catalytica, Inc. Catalyst structure having integral heat exchange
US5258349A (en) * 1990-11-26 1993-11-02 Catalytica, Inc. Graded palladium-containing partial combustion catalyst
US5259754A (en) * 1990-11-26 1993-11-09 Catalytica, Inc. Partial combustion catalyst of palladium on a zirconia support and a process for using it
US5281128A (en) * 1990-11-26 1994-01-25 Catalytica, Inc. Multistage process for combusting fuel mixtures
US5326253A (en) * 1990-11-26 1994-07-05 Catalytica, Inc. Partial combustion process and a catalyst structure for use in the process
US5425632A (en) * 1990-11-26 1995-06-20 Catalytica, Inc. Process for burning combustible mixtures
EP0819465A1 (en) * 1994-09-26 1998-01-21 Beijing Huaxia Environmental Protection Co. Exhaust gas catalyst comprising a supported noble metal containing composite oxide
WO2009105907A1 (en) * 2008-02-27 2009-09-03 Radiamon S.A. Catalytic radiating heating appliance
KR100987417B1 (en) 2008-11-11 2010-10-13 주식회사 영재 Catalyst heater

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5248251A (en) * 1990-11-26 1993-09-28 Catalytica, Inc. Graded palladium-containing partial combustion catalyst and a process for using it
US5250489A (en) * 1990-11-26 1993-10-05 Catalytica, Inc. Catalyst structure having integral heat exchange
US5258349A (en) * 1990-11-26 1993-11-02 Catalytica, Inc. Graded palladium-containing partial combustion catalyst
US5259754A (en) * 1990-11-26 1993-11-09 Catalytica, Inc. Partial combustion catalyst of palladium on a zirconia support and a process for using it
US5281128A (en) * 1990-11-26 1994-01-25 Catalytica, Inc. Multistage process for combusting fuel mixtures
US5326253A (en) * 1990-11-26 1994-07-05 Catalytica, Inc. Partial combustion process and a catalyst structure for use in the process
US5405260A (en) * 1990-11-26 1995-04-11 Catalytica, Inc. Partial combustion catalyst of palladium on a zirconia support and a process for using it
US5425632A (en) * 1990-11-26 1995-06-20 Catalytica, Inc. Process for burning combustible mixtures
US5511972A (en) * 1990-11-26 1996-04-30 Catalytica, Inc. Catalyst structure for use in a partial combustion process
EP0819465A1 (en) * 1994-09-26 1998-01-21 Beijing Huaxia Environmental Protection Co. Exhaust gas catalyst comprising a supported noble metal containing composite oxide
WO2009105907A1 (en) * 2008-02-27 2009-09-03 Radiamon S.A. Catalytic radiating heating appliance
KR100987417B1 (en) 2008-11-11 2010-10-13 주식회사 영재 Catalyst heater

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