JPS59208313A - Exothermic device - Google Patents

Exothermic device

Info

Publication number
JPS59208313A
JPS59208313A JP8378783A JP8378783A JPS59208313A JP S59208313 A JPS59208313 A JP S59208313A JP 8378783 A JP8378783 A JP 8378783A JP 8378783 A JP8378783 A JP 8378783A JP S59208313 A JPS59208313 A JP S59208313A
Authority
JP
Japan
Prior art keywords
fuel
combustion
porous body
ceramic porous
porous material
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
JP8378783A
Other languages
Japanese (ja)
Other versions
JPH0519043B2 (en
Inventor
Takeshi Matsumoto
松元 武志
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.)
Kyocera Corp
Original Assignee
Kyocera Corp
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 Kyocera Corp filed Critical Kyocera Corp
Priority to JP8378783A priority Critical patent/JPS59208313A/en
Publication of JPS59208313A publication Critical patent/JPS59208313A/en
Publication of JPH0519043B2 publication Critical patent/JPH0519043B2/ja
Granted legal-status Critical Current

Links

Abstract

PURPOSE:To provide a combustion device which is of a small size and light in weight and can perform safe combustion for a long time, by a method wherein contact oxidation reaction is made in gas fuel, produced by evaporating methanole, ethanole, ether, aceton, methane, buthane, etc., by means of a ceramic porous material by which a platinum group metal is carried. CONSTITUTION:The lower part of a fuel feed porous material 3 is conditioned to be immersed in fuel 2 stored in a fuel tank 1, and thereby the liquefied fuel 2 is sucked up by a capillary phenomenon, and almost of the fuel produces a gasified fuel during the suction process, and if a shutter 4 is opened, the fuel flows upward and is fed to a ceramic porous material 5 by which a catalyst component located above the shutter 4 is carried. Thereby, the gasified fuel performs oxidation reaction, i.e., combustion by the action of platinum, being a catalyst component, within a ceramic porous material 5. Utilization of excellent oxidation catalyst action of a platinum group metal enables efficient combustion for a long time without needing an ignition source.

Description

【発明の詳細な説明】 本発明は液体燃料の気化カス、気体燃Flを燃焼させる
ようにした発熱装置に関ずろものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a heat generating device that burns vaporized residue of liquid fuel, gaseous fuel Fl.

−・般に液体燃料を燃焼させる方式としては綿やガラス
ウール、石綿などの繊維素を束にしたり、織布などで構
成したいわゆる“芯”にて吸い上げ、芯利の先αjfi
i部に別途の点火源を近づけ、吸い」二けられた燃料の
一部を気化燃焼さ−U、その熱でもって次の燃1′−1
を気化燃焼させることにより連続的に燃焼を継続させる
ようにした方式によるもの、あるいは噴霧状に燃料を賄
出させ別途設けた点火源によって着火して発熱量の大き
な燃焼火炎をf4るようにした燃焼方式などが一般的で
ある。
- Generally speaking, liquid fuel is burnt by bundling cellulose such as cotton, glass wool, or asbestos, or sucking it up with a so-called "wick" made of woven fabric, and then burning it at the tip of the core.
A separate ignition source is brought close to part i, and part of the ignited fuel is vaporized and combusted.
A method in which combustion is continued continuously by vaporizing and burning fuel, or a method in which fuel is supplied in the form of a spray and is ignited by a separately provided ignition source to produce a combustion flame with a large calorific value. Combustion methods are common.

ところが、上記の如き燃焼方式では、比較的大きな発熱
量か得られる反面、燃焼装置が大型化すること、点火源
を装備しなければならないこと、火炎か発生することに
より火災を誘起する恐れか大きいこと、微小な発熱量を
完全燃焼させることによって長時間にわたり継続燃焼さ
せるような装置を安価に得られないなど多くの欠点を有
するばか燃焼を効率的に燃焼させることが困難であった
However, although the combustion method described above can generate a relatively large amount of heat, it requires a large combustion device, requires an ignition source, and has a high risk of causing a fire due to the generation of flames. In addition, it has been difficult to efficiently combust ``baka-combustion'', which has many drawbacks such as the inability to obtain inexpensive equipment that allows continuous combustion over a long period of time by completely combusting minute amounts of heat.

本発明は上記に鑑みて開発した発熱装置であって小型軽
量で長時間に亘り、安全に燃焼させることができ、かつ
燃料を効率的に燃焼させるようにしたものである。
The present invention is a heat generating device developed in view of the above, which is small and lightweight, can burn safely for a long time, and burns fuel efficiently.

以下、本発明実施例を図によって具体的に詳述する。Hereinafter, embodiments of the present invention will be specifically described in detail with reference to the drawings.

第1図は本発明装置の基本構成図で、1は燃料2を貯溜
する燃料タンク、3は下方部が燃利2中(こ浸漬される
如く配置された燃料導出多孔体であり、この燃料導出多
孔体3は1インチ平方当り50〜500セル程度の気孔
を有するポーラス(多孔質)セラミックあるいは石綿、
グラスウール、カーホンファイバーなどの集束体でもっ
て構成される。
Fig. 1 is a basic configuration diagram of the device of the present invention, in which 1 is a fuel tank for storing fuel 2, 3 is a fuel outlet porous body arranged so that its lower part is immersed in the fuel 2; The derived porous body 3 is made of porous ceramic or asbestos having pores of about 50 to 500 cells per square inch.
It is composed of a bundle of glass wool, carphone fiber, etc.

まノこ4はシャッターで燃料導出多孔体3からの燃料導
出量を加減したり、供給を停止させる操作を行なうもの
である。5はセラミック多孔体て、このセラミ、り多孔
体5としては三角、四角、六角、円形など多数の空孔を
もったハニカム形状のもの、不定形状の空孔をもった三
次元網状をしたものなと各空孔か連通し、通気抵抗の比
較的小さいものであればよく、これら多孔質の物体に対
し、酸化触媒成分である白金(Pt)パラジウム(Pa
)ロジウム(、Rh)なとの白金族金属を1β容量当り
、0.5〜5g程度担持させて構成されている。
The mango 4 uses a shutter to adjust the amount of fuel delivered from the porous fuel delivery body 3 or to stop the supply. Reference numeral 5 denotes a ceramic porous body, and the ceramic porous body 5 has a honeycomb shape with a large number of pores such as triangular, square, hexagonal, circular, etc., or a three-dimensional network with irregularly shaped pores. The oxidation catalyst components, platinum (Pt), palladium (Pa
) Rhodium (, Rh) and other platinum group metals are supported in an amount of about 0.5 to 5 g per 1β capacity.

さらに6は被加多:些物体を収納する容器で、被加熱物
体の量、性状などによってこの容器6の形状はそれぞれ
に最も適した形状のものを使用ずれはよい。
Furthermore, 6 is a container for storing small objects to be heated, and the shape of this container 6 may be selected depending on the amount and properties of the objects to be heated.

次に上記のように構成された発熱装置の作動を説明する
。いま、燃料タンク1に貯溜された燃料2には燃料導出
多孔体3の下方部か浸漬された状態にあることから液体
状の燃料2は毛細管現象によって吸い上げられ、この吸
い上げられる過程において燃料のほとんどが、気化燃料
となり、シャッター4が開路している場合には、上昇し
てこのシャック−4の上部に配設され触媒成分が担持さ
れたセラミック多孔体5に送られる。そのため気化燃料
はセラミック多孔体5中において触媒成分である白金に
よる作用でもって酸化反応、すなわち燃焼を起こすこと
となる。このような気化燃料の酸化反応に伴って燃焼熱
が発生することから連続的に燃料導出多孔体3から送ら
れてくる気化燃料はセラミ’7り多孔体5において酸化
反応が促進、拡大され連続的に酸化燃焼作用が絹(続す
ることになり、そのため発生した燃焼熱によって容器6
を加熱することから該容器6に入れられた被加熱物体(
図示せず)を加熱する。
Next, the operation of the heat generating device configured as described above will be explained. Now, since the fuel 2 stored in the fuel tank 1 is immersed in the lower part of the fuel derivation porous body 3, the liquid fuel 2 is sucked up by capillary action, and in this sucking process, most of the fuel is becomes vaporized fuel, and when the shutter 4 is open, it rises and is sent to the ceramic porous body 5 disposed in the upper part of the shack 4 and carrying catalyst components. Therefore, the vaporized fuel undergoes an oxidation reaction, that is, combustion, in the ceramic porous body 5 due to the action of platinum, which is a catalyst component. Combustion heat is generated along with the oxidation reaction of the vaporized fuel, so the oxidation reaction of the vaporized fuel continuously sent from the fuel deriving porous body 3 is promoted and expanded in the ceramic porous body 5, and the vaporized fuel is continuously As a result, the oxidative combustion effect continues on the silk, and the generated combustion heat causes the container 6 to
The object to be heated (
(not shown).

一方、白金族を担持させたセラミック多孔体5におりる
酸化反応を起こす容量が充分に大きい場合には、発生ず
る熱量は供給される気化燃料量にほぼ比例することから
、シャ・ツタ−4の開度を調節することによって発熱量
、力瞳シ温度を制御することができ、また該シャ・ツタ
−4を閉塞することによって発熱作動を停止させること
ができる。
On the other hand, if the capacity of the ceramic porous body 5 carrying platinum group metals to cause an oxidation reaction is sufficiently large, the amount of heat generated is approximately proportional to the amount of vaporized fuel supplied. By adjusting the degree of opening of the shutter 4, the amount of heat generated and the temperature of the shutter can be controlled, and by closing the shutter 4, the heat generating operation can be stopped.

ところで、上記の如く本発明発熱装置にて燃焼に供する
液体燃料としては1気圧下にお番フる611点が30°
C以上のメタノール(64°C)、エタノール(78°
C)エーテル(34’C)、アセトン(54℃)など比
較的低011点のOJ燃性有機液体を用いることが好ま
しくその他、カッリン、灯油などでもよいが、灯油の如
く沸点か比較的高いようなものにあっては第2図(a)
(b)にて例示するようにヒータIIを燃料導出多孔体
3、セラミ・ツク多孔体5なとの各々に埋設しておき、
該ヒータ11にバ・ノテリーI3より通電し加熱するこ
とによって一層酸化燃焼反応を促進させることかできる
By the way, as mentioned above, for the liquid fuel to be combusted in the heat generating device of the present invention, the 611 points at which the liquid fuel is combusted under 1 atm are 30 degrees.
Methanol (64°C), ethanol (78°C)
C) It is preferable to use an OJ flammable organic liquid with a relatively low 011 point, such as ether (34'C) or acetone (54°C).Also, kerosene, kerosene, etc. may be used; Figure 2 (a) for things
As illustrated in (b), the heater II is embedded in each of the fuel derivation porous body 3 and the ceramic porous body 5,
The oxidation combustion reaction can be further promoted by heating the heater 11 by supplying electricity from the battery I3.

さらに、燃焼に供する燃料としてはアルコーノ1ノ、エ
ーテル、アセトンなど常温常圧にて液体であるものに限
らず、加圧下において液体となり常温常圧では気体であ
るブタン、エタン、メクンなとの燃料を使用してもよく
、この場合供給される気体燃料の流れを整流するために
燃料導出多孔体3を具備させておいてもよいが、その場
合にりj必ずしも必要とはしない。
Furthermore, the fuels to be used for combustion are not limited to those that are liquid at room temperature and normal pressure, such as alconite, ether, and acetone, but also fuels that become liquid under pressure and gaseous at room temperature and normal pressure, such as butane, ethane, and mekun. In this case, a porous fuel outlet body 3 may be provided to rectify the flow of the supplied gaseous fuel, but it is not necessarily necessary in this case.

次に本発明装置のついての実験例を第1表に挙げる。Next, Table 1 lists experimental examples using the apparatus of the present invention.

これらA−Gの実験例における、特に燃焼反応の立上り
をセラミック多孔体5の中心点直上的5mmの位置の温
度と、燃料をセラミック多孔体5乙こ供給開始時点から
の経過時間とによりプロ・ノドしたのが第3図のグラフ
であって、これから明らかなように同一燃料を使用した
ものにおいて、仏事」導出多孔体3、セラミック多孔体
5の気孔率の大きなもの、すなわぢセル数が多く、かつ
大きな体積をもった、特にセラミック多孔体5を装備し
たものの方が温度立上りが早く、しかも高温度がi;、
′られる傾向か認められる。これば実験例Δ、B、Cか
ら明らかなように気化燃料と触媒成分を1u持第]−表 した部分との接触面積が多く、酸化反応か惣激に1だ進
されるためであると考えられる。
In these experimental examples A-G, the rise of the combustion reaction can be determined by controlling the temperature at a position 5 mm directly above the center point of the porous ceramic body 5 and the elapsed time from the time when the fuel starts being supplied to the porous ceramic body 5. What I found interesting was the graph in Figure 3.As can be seen from the graph, when the same fuel was used, the porosity of Buddhist porous body 3 and ceramic porous body 5 was large, that is, the number of cells was large. Those equipped with ceramic porous bodies 5 that have a large volume and a large volume have a faster temperature rise, and a higher temperature i;,
'There is a tendency to be accepted. This is because, as is clear from the experimental examples Δ, B, and C, the contact area between the vaporized fuel and the catalyst component is large, and the oxidation reaction is accelerated. Conceivable.

ところか、実験例D−Gにお6フる如く、セラミック多
孔体5か小さな体積のものにあってはセル数が多いもの
であったとしても酸化反応の立上りは緩慢で、この場合
、温度上昇値も約70゛C程度までであって比較的低い
温度に加熱するだめの発!:工1装置の構成に適してい
ることがわかる。また実験例F、Gのように燃料’6%
度の低いものを用いたものでは酸化反応の立上りは極め
て緩慢なものであって、上昇温度も20〜40°C範囲
にとどまる。したかって同じ発熱装置であったとしても
供給する燃料の濃度によって得られる発か)量、上昇温
度を制御することか可能であることが判る。
On the other hand, as shown in Experimental Example D-G, the oxidation reaction starts slowly when the ceramic porous body 5 has a small volume even if the number of cells is large. The rise value is only about 70°C, so heating to a relatively low temperature is not recommended! : It can be seen that it is suitable for the configuration of the first equipment. Also, as in experimental examples F and G, the fuel '6%
When a low temperature is used, the rise of the oxidation reaction is extremely slow, and the temperature rise remains within the range of 20 to 40°C. Therefore, even if the heating device is the same, it is possible to control the amount of heat generated and the temperature rise depending on the concentration of the supplied fuel.

なお、上記第1表に挙げた実験例には燃’A:Jとして
メタノールのみを用いた場合をあげたが、これに限らj
゛エタノールアセトンなど他の可燃性有1尺液体を用い
た場合もほぼ同様の温度上昇ずなわら酸化(燃焼)反応
をもつ傾向を示した。
Note that in the experimental examples listed in Table 1 above, only methanol was used as the fuel A:J;
゛When other flammable liquids such as ethanol acetone were used, almost the same tendency for oxidation (combustion) reaction was observed, although the temperature did not increase.

また、ブタンなど當温常圧状態で気体の燃料をセラミ、
り多孔体5に供給して酸化反応の立上りを調べたが、か
かる気体燃料を用いた場合にあってもほぼ同様の傾向が
見受りられた。ただし、沸点が高い液体燃料を用いる場
合と同様、初期の酸化反応を引起こすべく第3図(b)
の如くセラミック多孔体5中に埋設したヒータHてもっ
て予じめ加jlJ1すれば酸化反応を引起し継続させる
ことが容易に可能であった。
In addition, gaseous fuel such as butane at normal temperature and pressure can be mixed with ceramic,
The rise of the oxidation reaction was investigated by supplying gaseous fuel to the porous body 5, and almost the same tendency was observed even when such gaseous fuel was used. However, as in the case of using liquid fuel with a high boiling point, in order to cause an initial oxidation reaction,
It was easily possible to cause and continue the oxidation reaction by applying heat in advance using a heater H embedded in the ceramic porous body 5 as shown in FIG.

ところで、燃オ′−1を酸化反応(燃焼)させるセラミ
ック多孔体5としては充分な反応を起させるために可能
な限り体積の大きなものて、か゛つ11容蛍当り少くと
も酸化触媒としての白金族金属を0゜5〜5g担持させ
たものであるが、セル数として6;j、20〜600セ
ル/ R1のものが本発明発熱装置の構成に通ずるとと
もに使用に便利なものであった。
By the way, the ceramic porous body 5 for oxidizing (combusting) the combustible gas must have as large a volume as possible in order to cause a sufficient reaction. Although 0.5 to 5 g of group metal was supported, a cell number of 6;j and 20 to 600 cells/R1 was compatible with the structure of the heat generating device of the present invention and was convenient to use.

なお、本発明実施例においては燃料導出多孔体3とセラ
ミック多孔体5とをそれぞれ別体のもので構成したか、
これにl(Nらず、例えば一体のセラミック多孔質体を
用い、燃′A′、−1タンク1中の燃料2に’/l ’
IN シ、該燃料2を吸い上り、気化させる下半分は白
金族金属を担持さ一ヒす、下半分で気化した気化燃料を
酸化反応(燃焼)させるべく」二半分に対しては白金族
金属を担持させたものであってもよい。この場合におけ
る燃焼作動の開始、停止には酸化反応を行うセラミック
多孔体の部位への酸素(空気)の供給を遮断するように
するか、あるいは液体燃料への浸漬し燃料導出多孔体を
成す部分か燃料液面より離れる如くセラミック多孔質体
全体を上下方向にあげさけできるようにしたものであっ
てもよい。
In addition, in the embodiment of the present invention, the fuel deriving porous body 3 and the ceramic porous body 5 are constructed as separate bodies, respectively.
This is done by using l(N, for example, an integrated ceramic porous body, and adding '/l' to the fuel 2 in the fuel 'A', -1 tank 1.
In order to carry out an oxidation reaction (combustion) of the vaporized fuel in the lower half, the lower half that sucks up the fuel 2 and vaporizes it carries a platinum group metal. It may be supported. In this case, to start and stop the combustion operation, either cut off the supply of oxygen (air) to the part of the ceramic porous body that undergoes the oxidation reaction, or immerse the part in liquid fuel to form the fuel-delivery porous body. Alternatively, the entire ceramic porous body may be raised vertically away from the fuel liquid level.

なお、酸化反応を起させるセラミック多孔体の上部に配
置される容器6の形状は該容器6にて加熱される被加熱
物体を入れるに適したものであれば、特定する必要はな
く任意形状のものを用いればよい。
The shape of the container 6 placed above the ceramic porous body that causes the oxidation reaction does not need to be specified and can be of any shape as long as it is suitable for containing the object to be heated in the container 6. Just use something.

以上のよ・うに本発明によれば気体燃料あるいは液体燃
料で気化したものをセラミック多孔体に担持−已しめた
白金族金属の有するずくれた酸化触媒作用を利用するよ
うにした装置であることから、点火源を要せず小型軽量
で長時間に亘り、効率良(燃焼させることができ、しか
も火災などを引起こす恐れのない安全で多方面に使用し
得る発熱装置を安価に提(J(することができるなど多
くのすくれた特徴をもっている。
As described above, according to the present invention, it is a device that utilizes the unique oxidation catalytic action of platinum group metals, which support vaporized gaseous fuel or liquid fuel on a ceramic porous body. Therefore, we have proposed a low-cost heat generating device that does not require an ignition source, is small and lightweight, can be burned for a long time, is efficient (combustible), and is safe and can be used in many ways without the risk of causing a fire. (It has many cool characteristics, such as being able to

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

第1図は本発明実施例による発熱装置の縦断面図、第2
図(a)(b)は第1図における燃料導出多孔体3、セ
ラミック多孔体5のみのそれぞれ他の実施例を示す破断
面図である。第3図は本発明装置を用いた実験例による
上昇温度と反応時間の関係を示すグラフである。 ■=燃料タンク    2:液体燃料 3:燃料導出多孔体  4:シャノクー5:セラミック
多孔体 6:容器 出願人  京 セ ラ 株 式 会 社代表者 稲盛和
夫 第1図 第2図 (G)
FIG. 1 is a longitudinal sectional view of a heat generating device according to an embodiment of the present invention, and FIG.
Figures (a) and (b) are broken sectional views showing other embodiments of only the fuel deriving porous body 3 and the ceramic porous body 5 in FIG. 1, respectively. FIG. 3 is a graph showing the relationship between increased temperature and reaction time in an experimental example using the apparatus of the present invention. ■=Fuel tank 2: Liquid fuel 3: Fuel derivation porous body 4: Shanokou 5: Ceramic porous body 6: Container applicant Kyocera Co., Ltd. Company representative Kazuo Inamori Figure 1 Figure 2 (G)

Claims (1)

【特許請求の範囲】[Claims] メタノール、エタノール、エーテル、アセトン、メタン
、エタン、メタンなどの燃料を入れた燃料タンクと、該
燃料タンク中の燃料を導く燃料導出多孔体を介してプラ
チナ、パラジウムなどの白金族金属を担持させたセラミ
、り多孔体を配設せしめ、上記燗、料導出多孔体の上端
より放出される気化燃料を上記セラミック多孔体でもっ
て燃焼させるようにしたことを?IS徴とする発熱装置
Platinum group metals such as platinum and palladium are supported through a fuel tank containing fuel such as methanol, ethanol, ether, acetone, methane, ethane, and methane, and a fuel outlet porous body that guides the fuel in the fuel tank. A ceramic porous body is provided, and the vaporized fuel released from the upper end of the above-mentioned warm material deriving porous body is combusted by the ceramic porous body. A heat generating device that is a sign of IS.
JP8378783A 1983-05-12 1983-05-12 Exothermic device Granted JPS59208313A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8378783A JPS59208313A (en) 1983-05-12 1983-05-12 Exothermic device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8378783A JPS59208313A (en) 1983-05-12 1983-05-12 Exothermic device

Publications (2)

Publication Number Publication Date
JPS59208313A true JPS59208313A (en) 1984-11-26
JPH0519043B2 JPH0519043B2 (en) 1993-03-15

Family

ID=13812348

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8378783A Granted JPS59208313A (en) 1983-05-12 1983-05-12 Exothermic device

Country Status (1)

Country Link
JP (1) JPS59208313A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61280304A (en) * 1985-06-04 1986-12-10 Masao Sugiyama Heater
JPH0334518U (en) * 1989-08-08 1991-04-04
DE10042479A1 (en) * 2000-08-29 2002-03-14 Aral Ag & Co Kg Catalytic fuel oxidation reactor for heating duties in conventional vehicles, or for use as reformer or in chemical plant, has capillary section followed by catalyst

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5135009U (en) * 1974-09-09 1976-03-16
JPS5732332U (en) * 1980-03-25 1982-02-20
JPS5866707A (en) * 1981-10-16 1983-04-21 Matsushita Electric Ind Co Ltd Burner

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5135009U (en) * 1974-09-09 1976-03-16
JPS5732332U (en) * 1980-03-25 1982-02-20
JPS5866707A (en) * 1981-10-16 1983-04-21 Matsushita Electric Ind Co Ltd Burner

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61280304A (en) * 1985-06-04 1986-12-10 Masao Sugiyama Heater
JPH0231283B2 (en) * 1985-06-04 1990-07-12 Masao Sugyama
JPH0334518U (en) * 1989-08-08 1991-04-04
DE10042479A1 (en) * 2000-08-29 2002-03-14 Aral Ag & Co Kg Catalytic fuel oxidation reactor for heating duties in conventional vehicles, or for use as reformer or in chemical plant, has capillary section followed by catalyst

Also Published As

Publication number Publication date
JPH0519043B2 (en) 1993-03-15

Similar Documents

Publication Publication Date Title
JPS59208313A (en) Exothermic device
JPS61180818A (en) Hot air generation by catalytic burning
JP3054533B2 (en) Fuel cell system
US1176172A (en) Alcohol-stove.
JPH0113229Y2 (en)
JP2006501435A (en) Post-combustion device
JPS643952Y2 (en)
JPS60120114A (en) Catalystic burner
JP3880940B2 (en) Ignition device for catalytic oxidizer used in places where fire is restricted
JPS584006Y2 (en) Combustor with catalyst
JPH0579220U (en) Heat generating device and warmer using the same
JPS60202224A (en) Catalyst burner
JPH0477201B2 (en)
JPS6379707A (en) Burner of reformer for fuel cell
JPS602812A (en) Liquid fuel combustion device
JP3860262B2 (en) Catalytic combustion device
JPS6137524B2 (en)
JP2004035308A (en) Partial oxidation reforming apparatus
JPH01269806A (en) Fuel gasification device
JPS61184319A (en) Method of generating hot blast by catalytic combustion
JPS62213605A (en) Kerosene heater having double wick structure
TW200846603A (en) Energy-saving device and method for combustion with use of catalyst
JPS6379703A (en) Burner of reformer for fuel cell
JPS61119909A (en) Liquid fuel catalyst burner
JPS6176819A (en) Combustion device