JPS5831203A - Combustion wick - Google Patents

Combustion wick

Info

Publication number
JPS5831203A
JPS5831203A JP12995081A JP12995081A JPS5831203A JP S5831203 A JPS5831203 A JP S5831203A JP 12995081 A JP12995081 A JP 12995081A JP 12995081 A JP12995081 A JP 12995081A JP S5831203 A JPS5831203 A JP S5831203A
Authority
JP
Japan
Prior art keywords
fuel
surfactant
paint
wick
active agent
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
JP12995081A
Other languages
Japanese (ja)
Other versions
JPS6333608B2 (en
Inventor
Yasushi Hirata
康 平田
Kinichi Adachi
足立 欣一
Hisanori Nishiguchi
西口 久則
Yoshizo Omukae
大迎 淑三
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 JP12995081A priority Critical patent/JPS5831203A/en
Priority to US06/366,168 priority patent/US4421477A/en
Priority to CA000400701A priority patent/CA1196565A/en
Priority to DE8282103050T priority patent/DE3264865D1/en
Priority to EP82103050A priority patent/EP0062910B1/en
Priority to KR1019820001561A priority patent/KR830010341A/en
Priority to AU82539/82A priority patent/AU536532B2/en
Publication of JPS5831203A publication Critical patent/JPS5831203A/en
Publication of JPS6333608B2 publication Critical patent/JPS6333608B2/ja
Granted legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F23COMBUSTION APPARATUS; COMBUSTION PROCESSES
    • F23DBURNERS
    • F23D3/00Burners using capillary action
    • F23D3/02Wick burners
    • F23D3/08Wick burners characterised by shape, construction, or material, of wick

Abstract

PURPOSE:To obtain stable combustion for a wick, by determining a specific value as the rate of surface-active agent occupied in a coating material, as well as to impregnate a fuel vaporizing part, made of ceramic fiber, with the coating material, made of inorganic pigment, silica, and surface-active agent. CONSTITUTION:A main wick is made of ceramic fiber of silica-alumina system, added with polyacrylic ester. A fuel vaporizing part 3 is impregnated with coating material, made of inorganic pigment, silica, and surface-active agent, and the rate of surface-active agent occupied in the coating material is 0.2-5%. With such an arrangement, generation and accumulation of tar material are inhibited, so that stable combustion can be obtained for a wick for a long time.

Description

【発明の詳細な説明】 本発明は液体燃料用燃焼器に用いられる燃焼芯に関する
もので、その目的は燃焼芯の燃料気化部におけるタール
状物質の生成蓄積を抑え、長期間安定な燃焼を維持し得
る燃焼芯を提供することにある。
Detailed Description of the Invention The present invention relates to a combustion wick used in a liquid fuel combustor, and its purpose is to suppress the generation and accumulation of tar-like substances in the fuel vaporization part of the combustion wick and maintain stable combustion for a long period of time. The purpose of the present invention is to provide a combustion wick that can be used.

液体燃料全燃焼芯の毛細管現象によって吸い上げ、乏0
゛燃焼芯の気化室内に露出している先端部分、即ち燃料
気化部の表面から液体燃料を気化させて燃焼器←める、
いわゆる吸い」二げ気化式の燃焼器21゛−“・ は、石油ストーブ、石油コンロ等に広く用いらnている
。この種の燃焼器では、燃料気化部が高温でかつ酸素の
介在する雰囲気に暴露さfているために、燃焼中におい
て燃料気化部に含有される燃料の一部が酸化9重合反応
等によってタール状物質となり、燃料気化部に蓄積さ扛
るという現象が容易に生じていた。特に燃料中に微量の
高沸点成分が混入したり(例えば灯油中に機械油、軽油
All liquid fuel is sucked up by the capillary action of the combustion wick, resulting in low
``The liquid fuel is vaporized from the tip part of the combustion wick exposed in the vaporization chamber, that is, the surface of the fuel vaporization part, and the liquid fuel is charged into the combustor.
The so-called double vaporization type combustor 21 is widely used in kerosene stoves, oil stoves, etc. In this type of combustor, the fuel vaporization section is heated to a high temperature and is in an oxygen-containing atmosphere. Because of the exposure to In particular, trace amounts of high-boiling components may be mixed into the fuel (for example, machine oil or light oil in kerosene).

サラダ油等が混入した場合)、あるいは燃料成分の一部
が変質(例えば灯油全長期間高温、あるいに直射日光下
に保存した時に生ずる酸化物、過酸化物、樹脂等)して
いる場合等には、前記タール状物質の生成、蓄積は著し
く増大するっこのクール状物質が燃料気化部に蓄積した
時、燃料気化部の表面あるいは内部の毛細管が閉塞さn
、燃料の吸上げや気化が阻害さする。このため燃料気化
量が異常に低下し、そnに伴い発熱量が著しく低下し、
燃焼室における空燃比を崩して臭気、ススや有1iな一
酸化炭素全多発する様な不具合會生じていた。tた点火
時には上記タール状物質によって燃料気化部の速かなる
温度)二昇、燃料気化量の増加が妨げら扛、安定燃焼に
至るに著しく長時間を有し、その間不安定過渡燃焼によ
る臭さ 気、スス、−酸化炭素等の発生全増太贅→でいた。更に
タール状物質が燃焼芯ととnk支持する金属部と全固着
させ、←帰÷の機緘伯働昨串不4丁 能4−−−船一燃焼芯を下げての消火操作全不能とする
様な危険な状態もあった。
(If salad oil etc. is mixed in), or if some of the fuel components have deteriorated (for example, oxides, peroxides, resins, etc. that are generated when kerosene is stored at high temperatures for a long period of time or under direct sunlight). The generation and accumulation of the tar-like substance increases significantly.When this cool substance accumulates in the fuel vaporization part, the capillary tubes on or inside the fuel vaporization part are blocked.
, fuel uptake and vaporization are inhibited. As a result, the amount of fuel vaporized decreases abnormally, and as a result, the calorific value decreases significantly.
The air-fuel ratio in the combustion chamber was disrupted, causing problems such as odor, soot, and carbon monoxide. At the time of ignition, the tar-like substance causes the temperature of the fuel vaporization part to rise rapidly, preventing an increase in the amount of fuel vaporization, and it takes an extremely long time to reach stable combustion, during which time the odor caused by unstable transient combustion is generated. There was a lot of growth caused by air, soot, carbon oxide, etc. Furthermore, the tar-like substance completely adhered to the combustion wick and the supporting metal parts, making it completely impossible to extinguish the fire by lowering the combustion wick on the ship. There were some dangerous situations.

本発明はこ扛ら従来の欠点を解消するために、タール状
物質の生成蓄積を抑制するもので、以下本発明の一実施
例を添付図面と共に説明する。
The present invention aims to suppress the generation and accumulation of tar-like substances in order to eliminate these conventional drawbacks.One embodiment of the present invention will be described below with reference to the accompanying drawings.

第1図において、1は生花で、シリカ−アルミナ系のセ
ラミック繊維(シリカ:アルミナ=450:502重量
比)盆、有機バインダーの一例として用いたポリアクリ
ル酸エステルケ加えて形成したものである。2は吸−ヒ
げ芯で、ポリプロピレン布よりなり、生花1に連接さn
ている。3は主意1土部に形成した燃料気化部で、燃焼
器に装着した時、燃焼室に露出さ扛る部分である。燃料
気化部3には、無機顔料、無水ケイ酸及び界面活性剤か
ら成る塗料全含浸させてあり、211)界面活性剤の塗
料に占める割合は0.2〜6%である。4は縫製糸、6
は接着テープである。
In FIG. 1, 1 is a fresh flower, which was formed by adding a tray of silica-alumina ceramic fiber (silica:alumina = 450:502 weight ratio) and polyacrylic acid ester used as an example of an organic binder. 2 is a sucker wick made of polypropylene cloth and connected to fresh flower 1.
ing. Reference numeral 3 indicates a fuel vaporization section formed in the base section 1, which is exposed to the combustion chamber when installed in the combustor. The fuel vaporization section 3 is completely impregnated with a paint consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant.211) The proportion of the surfactant in the paint is 0.2 to 6%. 4 is sewing thread, 6
is adhesive tape.

上記構成において、液体燃料は吸上げ芯2から生花1へ
と吸上げら扛、燃料気化部3表面から気化する。ここで
本実施例の効果を燃料の流れとともに、従来例、および
塗料に占める界面活性剤の割合と比較して詳述する。
In the above configuration, the liquid fuel is sucked up from the suction wick 2 to the fresh flower 1 and vaporized from the surface of the fuel vaporization section 3. Here, the effects of this example will be explained in detail in comparison with the flow of fuel, the conventional example, and the proportion of surfactant in the paint.

第2図は従来のセラミック繊維のみからなる燃料気化部
3.第3図は燃料気化部3に、無機顔料。
FIG. 2 shows a conventional fuel vaporizing section 3 made of only ceramic fibers. Figure 3 shows an inorganic pigment in the fuel vaporization section 3.

無水ケイ酸及び界面活性剤から成る塗料を含浸させたも
ので、界面活性剤の塗料に占める割合を0・1チとした
もので、第4図は燃料気化部3に、前記塗料を含浸させ
たもので、界面活性剤の塗料に占める割合全1チとした
もの、第5図は燃料気化部3に、前記塗料を含浸させた
もので、界面活性剤の塗料に占める割合全10%とした
ものであり、おのおのその断面ケ示す。
It is impregnated with a paint consisting of silicic anhydride and a surfactant, and the ratio of the surfactant to the paint is 0.1. Fig. 4 shows a fuel vaporization section 3 impregnated with the paint. Figure 5 shows a case in which the fuel vaporization section 3 is impregnated with the paint, and the total proportion of surfactant in the paint is 10%. A cross section of each is shown.

即ち、燃料F(実線矢印)は主意1内を吸上げら扛、燃
料気化部3表面から気化する。このとき従来例において
は、第2図に示す」:うに、燃料Fは燃料気化部3先端
より多量に気化する。しかし燃料中の微量の高沸点成分
や変質成分は容易に気化しない。このため、この先端に
高沸点成分や変質成分籾蓄積し、温度と酸素の影響を受
はタール状物質T(白抜き矢印)に変化し、蓄積した。
That is, the fuel F (solid arrow) is sucked up inside the main body 1 and vaporized from the surface of the fuel vaporization section 3. At this time, in the conventional example, as shown in FIG. 2, a large amount of the fuel F is vaporized from the tip of the fuel vaporizing section 3. However, trace amounts of high-boiling components and degraded components in the fuel do not easily vaporize. For this reason, high-boiling components and altered components of the rice were accumulated at this tip, and under the influence of temperature and oxygen, they changed into a tar-like substance T (white arrow) and accumulated.

また、第3図に示すように、界面活性剤の塗料に占める
割合ケ0.1係とした場合、塗料は、食用の有機バイン
ダーを含んだシリカ−アルミナ系セラミック繊維には、
浸透しにりく、燃料気化部3表面に、多量に吸着し易い
。このため、燃料気化部3表面の気孔径は小となりすぎ
、気化量は著しく減少する。このことにより、発熱量が
著しく減少し、気孔もタール成分で閉塞さ扛易い状態と
なる不具合が生じた。ところが、第4図に示すように、
界面活性剤の塗料に占める割合全1チとした場合、塗料
は、セラミック繊維にある程度は浸透するため、燃料気
化部3表面の気孔径に小さくなりすぎず、また気化量も
減少するが、著(〜く発熱量が減少することはない。こ
のため、燃料気化部3にお6ベー=パ いて気化量の減少に伴う、熱量の蓄積による燃料中の微
量の高沸点成分や変質成分の熱分解は、スムーズに進行
し、クール状物質等の蓄積は生じない。さらに、塗料中
の無機顔料や無水ケイ酸は、一種の酸化触媒であり、そ
の触媒作用によって、この熱分解作用は促進さnる。し
かし、第6図に示すように界面活性剤の塗料に占める割
合i10係とした場合、塗料は、セラミック繊維に浸透
しすぎるため、燃料気化部3表面の気孔径が小となるだ
けでなく燃料気化部3内部の気孔径も小となるため、燃
料Fは、気化部表面への供給不足となり、気化部内部で
のタール蓄積もし易くなる。さらに、界面活性剤の量が
犬となるため、界面活性剤それ自身がタールの成因とな
る不具合も顕著となる。
Furthermore, as shown in Figure 3, when the proportion of surfactant in the paint is set to 0.1, the paint is
It is difficult to penetrate, and a large amount is easily adsorbed on the surface of the fuel vaporization section 3. Therefore, the pore diameter on the surface of the fuel vaporization section 3 becomes too small, and the amount of vaporization decreases significantly. This caused a problem in that the calorific value decreased significantly and the pores were also easily clogged with tar components. However, as shown in Figure 4,
When the proportion of surfactant in the paint is 1, the paint penetrates into the ceramic fibers to some extent, so the pore size on the surface of the fuel vaporization section 3 does not become too small, and the amount of vaporization decreases significantly. (The calorific value does not decrease. Therefore, as the amount of vaporized gas is reduced by pumping into the fuel vaporization section 3, the heat of trace amounts of high boiling point components and altered components in the fuel due to the accumulation of heat amount. The decomposition proceeds smoothly and no accumulation of cool substances occurs.Furthermore, the inorganic pigments and silicic anhydride in the paint are a type of oxidation catalyst, and their catalytic action accelerates this thermal decomposition action. However, when the proportion of the surfactant in the paint is set to i10 as shown in Figure 6, the paint penetrates into the ceramic fibers too much, and the pore size on the surface of the fuel vaporization section 3 becomes smaller. In addition, the pore diameter inside the fuel vaporization section 3 becomes smaller, resulting in insufficient supply of fuel F to the surface of the vaporization section, and tar accumulation inside the vaporization section becomes easy.Furthermore, if the amount of surfactant is Therefore, the problem that the surfactant itself causes tar becomes noticeable.

ちなみに吸上げ気化方式の石油燃焼器を用いて燃焼させ
たときの結果を示すと第6図のようになる。燃料は白灯
油にザラダ油i0.1容量チ混合させたものケ用い、燃
焼芯は以下の4種を用いた。
Incidentally, Figure 6 shows the results of combustion using a suction vaporization type oil combustor. The fuel used was a mixture of white kerosene and 0.1 volume of sarada oil, and the following four types of combustion wicks were used.

(1)燃料気化部3をシリカ−アルミナ系七ラミッり繊
維で形成し、未処理のもの。
(1) The fuel vaporization section 3 is made of silica-alumina heptamyl fiber and is untreated.

(2)上記(1)の燃料気化部3に、無機顔料、無水ケ
イ酸及び界面活性剤からなる塗料會含浸させたもので、
界面活性剤の塗料に占める割合’(r−Q、1チとした
もの。
(2) The fuel vaporization section 3 of (1) above is impregnated with a coating composition consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant,
Ratio of surfactant in paint (r-Q, 1 inch).

(3)  上記(1)に(2)と同じ塗料孕含浸させた
もので、界面活性剤の塗料に占める割合全1チとしたも
の。
(3) The above (1) is impregnated with the same paint as in (2), and the total proportion of surfactant in the paint is 1.

(4)上記(1) K (2)の塗料全含浸させたもの
で、界面活性剤の塗料に占める割合を10%としたもの
(4) Completely impregnated with the paint of (1) K (2) above, with the proportion of surfactant in the paint being 10%.

この4種を比較すると、第6図に示すように、界面活性
剤の割合を1チとしたもの(3)は、未処理のもの(1
)、界面活性剤の割合上0.1%としたもの(2)、界
面活性剤の割合を10%としたもの(4)に比べて発熱
量の低下が著しく減少している。
Comparing these four types, as shown in Figure 6, the one with a surfactant ratio of 1 (3) is different from the untreated one (1).
), the decrease in calorific value was significantly reduced compared to (2) where the proportion of surfactant was 0.1%, and (4) where the proportion of surfactant was 10%.

′−!た、界面活性剤の塗料に占める割合によって、発
熱■の低下に与える影響全比較すると、第7図に示すよ
うに、界面活性剤の割合が0.2〜6チのときにおいて
発熱量の維持特性が著しく良いことがわかる。
′-! In addition, when we compare the effects of the ratio of surfactant in the paint on the reduction of heat generation, as shown in Figure 7, when the ratio of surfactant is 0.2 to 6, the amount of heat generated is maintained. It can be seen that the characteristics are extremely good.

以上の様に本発明の燃焼芯は、セラミック繊維よりなる
燃料気化部に、無機顔料、無水ケイ酸及び界面活性剤か
ら成る塗料を含浸させたもので、界面活性剤の塗料に占
める割合’io、2〜5%とすることによって、タール
状物質の生成、蓄積上押え、長時間にわたって安定燃焼
が得られる。
As described above, the combustion wick of the present invention has a fuel vaporization section made of ceramic fibers impregnated with a paint consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant, and the ratio of the surfactant to the paint is 'io. , 2 to 5%, generation of tar-like substances, accumulation and suppression, and stable combustion over a long period of time can be obtained.

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

第1図は本発明の一実施例にかかる燃焼芯の部分断面図
、第2図〜第6図は燃焼芯の作用説明図、第6図、第7
図はその特性図である。 1・・・・・・主意、2・・・・・・吸上げ芯、3・・
・・・・燃料気化部。 代理人の氏名 弁理士 中 尾 敏 男 ほか1名第 
2 図 第3図
FIG. 1 is a partial sectional view of a combustion wick according to an embodiment of the present invention, FIGS. 2 to 6 are explanatory diagrams of the operation of the combustion wick, and FIGS.
The figure shows its characteristic diagram. 1... main intention, 2... suction wick, 3...
...Fuel vaporization section. Name of agent: Patent attorney Toshio Nakao and 1 other person
2 Figure 3

Claims (1)

【特許請求の範囲】[Claims] セラミック繊維に少量の有機・(イングーを加えて形成
した多孔体の燃料気化部の少なくとも一部に、無機顔料
、無水ケイ酸及び界面活性剤から成る塗料全含浸させ、
前記界面活性剤の塗料に占める割合’Io・2〜5%と
したことを特徴とする燃焼芯。
A paint consisting of an inorganic pigment, anhydrous silicic acid, and a surfactant is completely impregnated into at least a part of the fuel vaporization part of a porous body formed by adding a small amount of organic ingu to ceramic fibers,
A combustion wick characterized in that the proportion of the surfactant in the paint is 2 to 5%.
JP12995081A 1981-04-13 1981-08-19 Combustion wick Granted JPS5831203A (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP12995081A JPS5831203A (en) 1981-08-19 1981-08-19 Combustion wick
US06/366,168 US4421477A (en) 1981-04-13 1982-04-07 Combustion wick
CA000400701A CA1196565A (en) 1981-04-13 1982-04-08 Combustion wick
DE8282103050T DE3264865D1 (en) 1981-04-13 1982-04-08 Combustion wick
EP82103050A EP0062910B1 (en) 1981-04-13 1982-04-08 Combustion wick
KR1019820001561A KR830010341A (en) 1981-04-13 1982-04-09 Combustion wick
AU82539/82A AU536532B2 (en) 1981-04-13 1982-04-13 Wick for burner

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12995081A JPS5831203A (en) 1981-08-19 1981-08-19 Combustion wick

Publications (2)

Publication Number Publication Date
JPS5831203A true JPS5831203A (en) 1983-02-23
JPS6333608B2 JPS6333608B2 (en) 1988-07-06

Family

ID=15022439

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12995081A Granted JPS5831203A (en) 1981-04-13 1981-08-19 Combustion wick

Country Status (1)

Country Link
JP (1) JPS5831203A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62279803A (en) * 1986-05-13 1987-12-04 ヘキスト セラニーズ コーポレーション Liquid/liquid extraction by microporous membrane

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56146907A (en) * 1980-04-17 1981-11-14 Matsushita Electric Ind Co Ltd Liquid fuel combustion wick
JPS6136129A (en) * 1984-07-30 1986-02-20 Sumitomo Electric Ind Ltd Manufacture of glass preform for optical fiber

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS56146907A (en) * 1980-04-17 1981-11-14 Matsushita Electric Ind Co Ltd Liquid fuel combustion wick
JPS6136129A (en) * 1984-07-30 1986-02-20 Sumitomo Electric Ind Ltd Manufacture of glass preform for optical fiber

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62279803A (en) * 1986-05-13 1987-12-04 ヘキスト セラニーズ コーポレーション Liquid/liquid extraction by microporous membrane
JPH0767521B2 (en) * 1986-05-13 1995-07-26 ヘキスト セラニーズ コーポレーション Liquid / liquid extraction method with microporous membrane

Also Published As

Publication number Publication date
JPS6333608B2 (en) 1988-07-06

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